Geminal systems -: 50.: Synthesis and alcoholysis of N-acyloxy-N-alkoxy derivatives of ureas, carbamates, and benzamides

被引:19
|
作者
Shtamburg, VG
Klots, EA
Pleshkova, AP
Avramenko, VI
Ivonin, SP
Tsygankov, AV
Kostyanovsky, RG
机构
[1] Russian Acad Sci, NN Semenov Chem Phys Inst, Moscow 119991, Russia
[2] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 119991, Russia
[3] Dnepropetrovsk Natl Univ, UA-49050 Dnepropetrovsk, Ukraine
关键词
N-alkoxy-N-chloro derivatives of ureas; carbamates; benzamide; and p-toluenesulfonamide; sodium carboxylates; N-acyloxy-N-alkoxy derivatives of ureas; and tertiary alkylamines; alcoholysis; H-1 NMR spectra; mass spectra; N; N-dialkoxyamino derivatives of ureas and carbamates;
D O I
10.1023/B:RUCB.0000011887.40529.b0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Procedures were developed for the synthesis of N-acyloxy-N-alkoxy derivatives of ureas, carbamates, and benzamides by the reactions of the corresponding N-alkoxy-N-chloro derivatives with sodium carboxylates in MeCN. N-Chloro-N-etlioxy-p-toluenesulfonamide was inert in this reaction. Alcoholysis of N-acyloxy-N-alkoxy derivatives of ureas, carbamates, and tert-alkylamines afforded the corresponding N,N-dialkoxy derivatives, whereas alcoholysis of N-acetoxy-N-ethoxybenzamide gave rise to alkyl benzoates.
引用
收藏
页码:2251 / 2260
页数:10
相关论文
共 3 条
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    V. G. Shtamburg
    E. A. Klots
    A. P. Pleshkova
    V. I. Avramenko
    S. P. Ivonin
    A. V. Tsygankov
    R. G. Kostyanovsky
    [J]. Russian Chemical Bulletin, 2003, 52 : 2251 - 2260
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    KOSTYANOVSKII, RG
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    SHUSTOV, GV
    ZOLOTOI, AB
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    ATOVMYAN, LO
    VOZNESENSKII, VN
    KOSTYANOVSKII, RG
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