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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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