Synthesis of Imines from Amines in Aliphatic Alcohols on Pd/ZrO 2 Catalyst at Ambient Conditions

Σχετικά έγγραφα
Metal-free Oxidative Coupling of Amines with Sodium Sulfinates: A Mild Access to Sulfonamides

Supporting Information. Experimental section

Supporting Information

Copper-catalyzed formal O-H insertion reaction of α-diazo-1,3-dicarb- onyl compounds to carboxylic acids with the assistance of isocyanide

Divergent synthesis of various iminocyclitols from D-ribose

Electronic Supplementary Information

Supporting Information. Asymmetric Binary-acid Catalysis with Chiral. Phosphoric Acid and MgF 2 : Catalytic

A facile and general route to 3-((trifluoromethyl)thio)benzofurans and 3-((trifluoromethyl)thio)benzothiophenes

9-amino-(9-deoxy)cinchona alkaloids-derived novel chiral phase-transfer catalysts

Enantioselective Organocatalytic Michael Addition of Isorhodanines. to α, β-unsaturated Aldehydes

Protease-catalysed Direct Asymmetric Mannich Reaction in Organic Solvent

Direct Palladium-Catalyzed Arylations of Aryl Bromides. with 2/9-Substituted Pyrimido[5,4-b]indolizines

and Selective Allylic Reduction of Allylic Alcohols and Their Derivatives with Benzyl Alcohol

Supporting information

Copper-Catalyzed Oxidative Dehydrogenative N-N Bond. Formation for the Synthesis of N,N -Diarylindazol-3-ones

Room Temperature Highly Diastereoselective Zn-Mediated. Allylation of Chiral N-tert-Butanesulfinyl Imines: Remarkable Reaction Condition Controlled

Supporting Information. Experimental section

Free Radical Initiated Coupling Reaction of Alcohols and. Alkynes: not C-O but C-C Bond Formation. Context. General information 2. Typical procedure 2

Supporting Information

Copper-Catalyzed Direct Acyloxylation of C(sp 2 ) H Bonds. in Aromatic Amides

Supporting Information

Supporting information

Electronic Supplementary Information

Ferric(III) Chloride Catalyzed Halogenation Reaction of Alcohols and Carboxylic Acids using - Dichlorodiphenylmethane

The Free Internet Journal for Organic Chemistry

Supporting Information One-Pot Approach to Chiral Chromenes via Enantioselective Organocatalytic Domino Oxa-Michael-Aldol Reaction

Supporting Information

ESI for. A simple and efficient protocol for the palladium-catalyzed. ligand-free Suzuki reaction at room temperature in aqueous DMF.

Copper-Catalyzed Oxidative Coupling of Acids with Alkanes Involving Dehydrogenation: Facile Access to Allylic Esters and Alkylalkenes

Sotto, 8; Perugia, Italia. Fax: ; Tel: ;

Sequential catalysis for the production of sterically hindered amines: Ruthenium(II)-catalyzed C-H bond activation and hydrosilylation of imines

Supporting Information for

Regioselectivity in the Stille coupling reactions of 3,5- dibromo-2-pyrone.

Mandelamide-Zinc Catalyzed Alkyne Addition to Heteroaromatic Aldehydes

Supplementary Figure S1. Single X-ray structure 3a at probability ellipsoids of 20%.

Supporting Information

Lewis Acid Catalyzed Propargylation of Arenes with O-Propargyl Trichloroacetimidate: Synthesis of 1,3-Diarylpropynes

Electronic Supplementary Information

A straightforward metal-free synthesis of 2-substituted thiazolines in air

Supporting Information

Supporting Information

Supporting information

Supporting Information

Hiyama Cross-Coupling of Chloro-, Fluoroand Methoxy- pyridyl trimethylsilanes : Room-temperature Novel Access to Functional Bi(het)aryl

Heterobimetallic Pd-Sn Catalysis: Michael Addition. Reaction with C-, N-, O-, S- Nucleophiles and In-situ. Diagnostics

Supplementary Material

Supporting Information for Synthesis of Fused N-Heterocycles via Tandem C-H Activation

Site-Selective Suzuki-Miyaura Cross-Coupling Reactions of 2,3,4,5-Tetrabromofuran

The N,S-Bidentate Ligand Assisted Pd-Catalyzed C(sp 2 )-H. Carbonylation using Langlois Reagent as CO Source. Supporting Information.

Electronic Supplementary Information. Carbon dioxide as a reversible amine-protecting

Rh(III)-Catalyzed C-H Amidation with N-hydroxycarbamates: A. new Entry to N-Carbamate Protected Arylamines

Rhodium-Catalyzed Oxidative Decarbonylative Heck-type Coupling of Aromatic Aldehydes with Terminal Alkenes

Phosphorus Oxychloride as an Efficient Coupling Reagent for the Synthesis of Ester, Amide and Peptide under Mild Conditions

Direct Transformation of Ethylarenes into Primary Aromatic Amides with N-Bromosuccinimide and I 2 -aq NH 3

Supporting Information for

Design and Solid Phase Synthesis of New DOTA Conjugated (+)-Biotin Dimers Planned to Develop Molecular Weight-Tuned Avidin Oligomers

Supplementary Information

College of Life Science, Dalian Nationalities University, Dalian , PR China.

Supporting Information for Iron-catalyzed decarboxylative alkenylation of cycloalkanes with arylvinylic carboxylic acids via a radical process

First DMAP-mediated direct conversion of Morita Baylis. Hillman alcohols into γ-ketoallylphosphonates: Synthesis of

Supporting Information for

using metal-organic framework Cu-MOF-74 as an efficient heterogeneous catalyst Hanh T. H. Nguyen, Oanh T. K. Nguyen, Thanh Truong *, Nam T. S.

Electronic Supplementary Information (ESI)

Catalyst-free transformation of levulinic acid into pyrrolidinones with formic acid

Iodine-catalyzed synthesis of sulfur-bridged enaminones and chromones via double C(sp 2 )-H thiolation

Synthesis and evaluation of novel aza-caged Garcinia xanthones

Fluorinative Ring-opening of Cyclopropanes by Hypervalent Iodine Reagents. An Efficient Method for 1,3- Oxyfluorination and 1,3-Difluorination

Heavier chalcogenone complexes of bismuth(iii)trihalides: Potential catalysts for acylative cleavage of cyclic ethers. Supporting Information

Cu-Catalyzed/Mediated Synthesis of N-Fluoroalkylanilines from Arylboronic Acids: Fluorine Effect on the Reactivity of Fluoroalkylamines

Visible Light-Driven Oxidative Coupling Reactions of Amines. by Photoactive WS2 Nanosheets

Supporting Information

Electronic Supplementary Information

Aerobic cross-dehydrogenative coupling of terminal alkynes and tertiary amines by a combined catalyst of Zn 2+ and OMS- 2

Supporting Information. A catalyst-free multicomponent domino sequence for the. diastereoselective synthesis of (E)-3-[2-arylcarbonyl-3-

Supporting Information

Supporting Information

Supporting Information

1011 Σύνθεση του 1,4-δι-tert-βουτυλοβενζολίου από tertβουτυλοβενζόλιο και tert-βουτυλο χλωρίδιο

Supporting Information

Supporting Information for

Fast copper-, ligand- and solvent-free Sonogashira coupling in a ball mill

Supporting Information

Supporting Information

Kishore Natte, Jianbin Chen, Helfried Neumann, Matthias Beller, and Xiao-Feng Wu*

Supplementary!Information!

Supporting Information. Copyright Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006

Supporting Information

Efficient and Simple Zinc mediated Synthesis of 3 Amidoindoles

Synthesis of novel 1,2,3-triazolyl derivatives of pregnane, androstane and D-homoandrostane. Tandem Click reaction/cu-catalyzed D-homo rearrangement

Tributylphosphine-Catalyzed Cycloaddition of Aziridines with Carbon Disulfide and Isothiocyanate

Highly enantioselective cascade synthesis of spiropyrazolones. Supporting Information. NMR spectra and HPLC traces

SUPPORTING INFORMATION. Transition Metal-Free Arylations of In-Situ Generated Sulfenates with Diaryliodonium Salts

Chiral Brønsted Acid Catalyzed Enantioselective Intermolecular Allylic Aminations. Minyang Zhuang and Haifeng Du*

gem-dichloroalkenes for the Construction of 3-Arylchromones

Novel and Selective Palladium-Catalyzed Annulation of 2-Alkynylphenols to Form 2-Substituted 3-Halobenzo[b]furans. Supporting Information

phase: synthesis of biaryls, terphenyls and polyaryls

multicomponent synthesis of 5-amino-4-

Supplementary material

Facile construction of the functionalized 4H-chromene via tandem. benzylation and cyclization. Jinmin Fan and Zhiyong Wang*

Supporting Information

Transcript:

This journal is The Royal Society of Chemistry 213 Synthesis of Imines from Amines in Aliphatic Alcohols on Pd/ZrO 2 Catalyst at Ambient Conditions Wenjing Cui, a Bao Zhaorigetu,* a Meilin Jia, a and Wulan Ao, a Huaiyong Zhu b Figure S1. (a) TEM images and (b) size distribution of the 1%wtPd/ZrO 2 catalysts. Figure S2. XRD pattern of (a) 1 wt% Pd/ZrO 2 catalysts and (b) ZrO 2 Figure S3. X-ray photoelectron spectrum (XPS) of Pd 3d in 1 wt% Pd/ZrO 2

This journal is The Royal Society of Chemistry 213 Figure S4. Recyclability tests of Pd/ZrO 2 for the synthesis of imine from benzylamine and ethanol Table S1 The reaction of benzylamine with aliphatic alcohols on different catalysts a Yield (%) b Entry Aliphatic Alcohol 3 wt% Au/ZrO 2 3 wt% Pd/ZrO 2 3 wt% Au-Pd/ZrO 2 1 CH 3 OH(2b) 88 84 2 2a 34 97 94 3 CH 3 (CH 2 ) 2 OH(2c) 34 84 64 4 CH 3 (CH 2 ) 3 OH(2d) 46 83 83 CH 3 (CH 2 ) 4 OH(2e) 1 96 84 6 CH 3 (CH 2 ) OH(2f) 39 86 74 7 OH(2g) 77 86 8 OH(2h) 44 74 83 9 OH(2i) 33 1 9(76) c 1 OH (2j) 3 12 97 11 OH (2k) 33 3 97 12 C OH (2l) a Reaction conditions: 1 (1 mmol), 2 (1 ml), catalyst (1 mg), KOH (.1 mmol), air atmosphere, 3 C, 6h; b determined by GC; c reaction time 12 h.

This journal is The Royal Society of Chemistry 213 Experimental General. The mixture of amine 1a (1 mmol), alcohol 2a (1 ml), 1 wt% Pd/ZrO 2 (1 mg) and KOH (.1 mmol) was sealed under air in a ml tube, stirred at 3 C for 6 h. During the reactions.1 ml specimens were periodically sampled, filtered and analyzed by GC (Shimadzu GC-214) with a capillary column of Rtx- (3 m length,. mm internal diameter,. μm film thickness), temperature of column ranged from to 22 C (6 C/min), and injector temperature was 2 C and flame ionization detector was used for product analysis. All synthetic compounds are known, and they were identified by comparison with authentic samples. Selected products were purified by column chromatography on alumina gel (V petroleum ether: V ethyl acetate: V triethylamine was : 1: 1), and were analyzed by 1 H NMR. We compared their 1 H NMR spectra with the reported literature. GC-MS (Thermo DSQ Ⅱ) with a HP- column was also used to identify the products. Characterization of products and Rerference N-ethylidenebenzylamine Product 3aa (CAS registry No: 34233--) 1 H NMR ( MHz, MeOD) δ 7.74 (t, J =.2 Hz, 1H), 7.39 7.31 (m, H), 4.4 (s, 2H), 1.86 (dt, 3H) ppm. This compound was known: F. Texier-Boullet, Synthesis, 198, 679 681. N-propylidenebenzylamine Product 3ac (CAS registry No: 639--2): 1 H NMR ( MHz, MeOD) δ 7.82 (t, J =.2 Hz, 1H), 7.39 7.19 (m, H), 4.3 (s, 2H), 2.33 2.18 (m, 2H), 1.69 1.3 (m, 2H),.96 (t, J = 7.4 Hz, 3H) ppm. This compound was known: V. Coeffard, C. Thobie-Gautier, I. Beaudet, Eur. J. Org. Chem., 28, 383 391. N-butylidenebenzylamine Product 3ad (CAS registry No: 6249-61-7) 1 H NMR ( MHz, MeOD) δ 7.94 (t, 1H), 7. 7. (m, H), 4.4(s, 2H), 2.7 (td, J = 7., 1.2

This journal is The Royal Society of Chemistry 213 Hz, 2H), 1.71 (dt, J = 14., 7.2 Hz, 2H),.9 (t, J = 7.4 Hz, 3H). This compound was known: P. K. Khatri, S. L. Jain, L. N. Sivakumar K, Org. Biomol. Chem., 211, 9, 33 3374. Results of GC-MS: 3aa D #312- RT: 4.32-4.71 AV: 94 NL:.3E8.9 9 8 3 2 1 1. 89. 77. 14. 132. 118. 133.1 134.1 181.1 27. 221.1 267. 281. 29. 326.9 341. 382.9 398.9 1 2 2 3 3 3ab A #2 RT: 3.84 AV: 1 NL: 8.22E7 91. 3 2.1 119.1 1 89.1 12.1 146. 26.9 249.2 281.3 3.1 327.2 4.8 397.4 1 2 2 3 3 3ac

This journal is The Royal Society of Chemistry 213 A #449-61 RT: 4.-.38 AV: 113 NL: 2.61E8 91. 9 8 3 2 1 1. 89. 118.1 146.1 147.1 77. 14.1 148.1 11.1 193. 27.1 2.1 267.1 281.1 327. 341. 3. 38. 1 2 2 3 3 3ad F #748 RT: 6.17 AV: 1 NL: 1.2E9 118. 91. 9 8 3 2 1 1. 83. 77. 84.1 14. 132. 133.1 146.1 1.1 161.1 162.1 27. 221.1 267. 281. 3. 341. 3. 398.9 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3ae O #962 RT: 7.8 AV: 1 NL: 2.27E8 91.1 3af 9 8 3 2 1 1.1 89. 77. 1.1 146.1 147.1 132.1 1.1 1.1 27.1 221.2 266.2 281.1 311.1 327.1 7.3 382. 399.3 1 2 2 3 3 I #1324 RT: 8.61 AV: 1 NL: 3.26E7 91. 3 132.1 133.1 2. 146.1 1 89.1 1.2 189.1 27.1 2.2 281.4 328. 343.3 361.2 397.9 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3ag C #-629 RT:.46-.66 AV: NL: 9.79E8.9 3ah 9 8 3 2 1 1. 89. 77. 93.1 161.1 146.1 132. 118.1 162.1 163.2 27. 223. 2.1 281. 3. 341. 3. 397.1 1 2 2 3 3 14 #818 RT: 6.47 AV: 1 NL: 1.E8 91. 3 2. 132. 133.1 1 89. 1.1 1.1 27.3 266.1 2.6 333.6 374.9 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3ai E #4-616 RT:.-.61 AV: 63 NL: 4.1E8.9 9 8 3 2 1 1.1 89. 66. 77. 14.1 146.1 132.1 147.1 148.1 149.1 181.1 27. 238.1 267. 281.1 327. 341. 3. 399. 1 2 2 3 3 3aj B #672-88 RT:.8-6.64 AV: 187 NL: 2.34E8.9 9 8 3 2 1 1. 89. 77. 1.1 132. 1.1 161.1 162.1 163.1 27. 221.1 2.1 281. 29. 341. 3. 384.9 399. 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3ak C #961 RT: 7.7 AV: 1 NL: 8.28E7 91. 9 8 3 2 1 1.1 146.1 147.1 89. 77. 1.1 132.1 1.1 1.1 27.1 221. 267. 281.2 39.9 326.8 341. 382.7 1 2 2 3 3 3ba W #6 RT:.99 AV: 1 NL: 2.34E8 1. 3 127.1 2 89.1 167.1 1 63.1 99. 128.1 169.1 27.2 268.1 281.2 341.1 3.2 371.7 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3ca 1 #2 RT:.2 AV: 1 NL: 1.E8 1. 3 2 16.1 1 77.1 13.1 147.1 17.1 148.2 27.3 221.1 281.2 333.2 4.8 3. 1 2 2 3 3 3da V #869 RT: 6.68 AV: 1 NL: 7.3E7 121.1 3 2 1 77.1 122.1 163.2 91.1 123.1 164.2 198.3 221. 281.1 327.4 6.1 391.7 1 2 2 3 3 3ea X #837 RT: 6.4 AV: 1 NL: 3.3E7 121.1 122.1 91.1 3 2 77.1 163.2 1 16.1 123.2 164.2 27.2 232.2 267. 281.1 327. 3.3 376.2 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3fa 9 #7 RT: 6.24 AV: 1 NL: 4.E7 91.1 121. 163.2 3 2.1 93.1 1 132.1 119.1 164.2 26.9 22.9 281. 327.1 3.3 369.2 394.6 1 2 2 3 3 3ga T #433 RT: 4.83 AV: 1 NL: 4.E7 6.1 3ha 3 132.1 2 91.1 1.1 1 147.2 168.2 27.1 221.3 281.2 327. 341.1 38.9 1 2 2 3 3 Y #347 RT: 4.47 AV: 1 NL: 6.8E7 1.1 3 2 16.1 77.1 1 147.2 1.1 84. 132.1 149.2 27.2 221.1 281.2 327.3 3.1 382.9 1 2 2 3 3

This journal is The Royal Society of Chemistry 213 3ia U #2188 RT: 12.28 AV: 1 NL: 1.22E8 167.1 3 1.1 2 12.1 168.2 1 83.1 1.1 11.1 29.2 23.2 281. 33.7 341.2 9.6 387.2 1 2 2 3 3