Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66643생성일: 2026년 10월 24일
Chlorotrimethylsilane → 7-(Phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid
https://huagongshe.com/ko/reaction/66643
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Phenylacetyl chloride | HCID 7679 | — |
| 반응물 | Cephalothin Sodium | HCID 23675321 | — |
| 반응물 | Monosilyltrifluoroacetamide | HCID 123231972 | — |
| 생성물 | 7-(Phenylacetyl-2-thienylacetyl)amino-3-acetoxymethyl-3-cephem-4-carboxylic acid | HCID 88743706 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04342757 |
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| 출처 데이터셋 | uspto-grants-1982_08 |
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| ORD ID | ord-6ec1b66b982943509e0e77e0253e85ba |
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| 출처 메모 | uspto-grants-1982_08 |
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