Trifluoroacetic acid in the synthesis of thiolcarbamates and s-methyl alkanethioates
作者:
Yu.N.Polivin,
E.A.Ageev,
期刊:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science
(Springer Available online 2004)
卷期:
Volume 40,
issue 1
页码: 178-180
ISSN:0568-5230
年代: 2004
DOI:10.1007/BF00959656
出版商: Springer_US-Boston
数据来源: Springer
摘要:
The major products of the reaction of 2-bromohexanoic acid with methyl thiocyanate in trifluoroacetic acid are S-methyl 2-bromohexanethioate (II) (55% yield), S-methyl 2,2,2-trifluoroethanethioate (IV) (31% yield), N-trifluoro-acetyltrifluoroacetamide (V) (11% yield), and N-trifluoroacetyl-S-methylthiol-carbamate (III) (29% yield). N-2-Bromohexanoyl-S-methylthiolcarbamate (I), N-2-bromohexanoyltrifluoroacetaraide (VI), 2-thiapropioamide(VII), and S-methyl hex-anethioate (VIII) are also formed in minor amounts.
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