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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66694생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/66694

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물Phenylacetyl chlorideHCID 7679—
반응물Cephalothin SodiumHCID 23675321—
반응물MonosilyltrifluoroacetamideHCID 123231972—
생성물7-(Phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acidHCID 88743706—

반응 조건

온도45 °C

반응 단계

A suspension of sodium cephalothin (3.36 g.) in anhydrous alcohol-free chloroform (20 ml.) is silylated by the addition of trimethylchlorosilane (2.2 ml.). After stirring for 30 minutes, monosilyltrifluoroacetamide (5.0 ml.) and phenylacetyl chloride (4.0 ml.) are added and the mixture is then heated to 45° C. for two days under a condenser fitted with a drying tube. The volatiles are evaporated to afford a residue which is dissolved in 100 ml. of ethyl acetate and washed three times with water. The ethyl acetate layer is dried over magnesium sulfate, filtered and the solution evaporated in vacuo to a residue. The residue is triturated with chloroform, any insolubles are removed by filtration and the product precipitated from the filtrate with hexane. This procedure is followed two more times. The 7-(phenylacetyl-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 번호US04342869
출처 데이터셋uspto-grants-1982_08
ORD IDord-eba1bbbe819741b4b909534555e66d29
출처 메모uspto-grants-1982_08