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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66644생성일: 2026년 10월 25일

Chlorotrimethylsilane → 7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/66644

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물2-Thiopheneacetyl chlorideHCID 162362—
반응물Cephalothin SodiumHCID 23675321—
반응물MonosilyltrifluoroacetamideHCID 123231972—
용매ChloroformHCID 6212—
생성물7-(Di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 70541217—

반응 조건

온도45 °C

반응 단계

A suspension of sodium cephalothin (1.18 g.) in anhydrous alcohol-free chloroform (10 ml.) is silylated by the addition of trimethylchlorosilane (1.1 ml.). After stirring for 30 minutes, monosilyltrifluoroacetamide (2.5 ml.) and 2-thienylacetyl chloride (2.0 ml.) are added to the suspension which is then heated to 45° C. The mixture is allowed to remain at this temperature for two days and then evaporated in vacuo to a residue which is dissolved in ethyl acetate (50 ml.) and washed three times with water. The ethyl acetate layer is dried over magnesium sulfate, filtered and the filtrate evaporated in vacuo to obtained a residue. The residue is dissolved in chloroform and precipitated with hexane three times, each time discarding the supernatent liquid. The 7-(di-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid is obtained in a solvent-free form by freeze-drying from a solution in benzene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04342757
출처 데이터셋uspto-grants-1982_08
ORD IDord-5bd39d5c12d448c8a6d7ff4fbd656c60
출처 메모uspto-grants-1982_08