A green way to γ-lactams through a copper catalyzed ARGET-ATRC in ethanol and in the presence of ascorbic acid

被引:33
作者
Casolari, Roberto [1 ]
Felluga, Fulvia [2 ]
Frenna, Vincenzo [3 ]
Ghelfi, Franco [1 ]
Pagnoni, Ugo M. [1 ]
Parsons, Andrew F. [4 ]
Spinelli, Domenico [5 ]
机构
[1] Univ Modena & Reggio Emilia, Dipartimento Chim, I-41125 Modena, Italy
[2] Univ Trieste, Dipartimento Sci Chim, I-34127 Trieste, Italy
[3] Univ Palermo, Dipartimento Chim Organ E Paterno, I-90128 Palermo, Italy
[4] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[5] Alma Mater Studiorum, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
关键词
Halocompounds; ATRC; gamma-Lactams; CuCl; Ascorbic acid; TRANSFER RADICAL-ADDITION; ELECTRON-TRANSFER; FUNCTIONAL REARRANGEMENT; CYCLIZATION REACTIONS; METHYL-METHACRYLATE; STEREOSELECTIVE-SYNTHESIS; KHARASCH ADDITION; ORGANIC-SYNTHESIS; MOLECULAR-WEIGHT; CHAIN REACTIONS;
D O I
10.1016/j.tet.2010.11.025
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A 'green' ARGET-ATRC, for the CuCl[PMDETA] catalysed cyclo-isomerization of N-allyl-alpha-polychloroamides to gamma-lactams is described. The process works efficiently (yields 78-96%), uses a bio-solvent, as ethanol, and exploits the reducing feature of ascorbic acid to limit, at a low level (2-4%), the amount of catalyst. To preserve the efficacy of the catalytic cycle, addition of Na2CO3 is essential, which quenches the HCl released during the CuCl[PMDETA] regeneration step. Profitable features of the process are: mild reaction temperatures (25-37 degrees C), relatively short reaction times (usually 5 h) and low solvent volumes (2 mmol of substrate/mL of ethanol). The method, upon stoichiometric adjustment, was also used for the synthesis of alpha,beta-unsaturated-gamma-lactams from N-(2-chloroallyl)-alpha-polychloroamides, via a tandem process involving an ATRC and a reductive [1,2]-elimination. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:408 / 416
页数:9
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