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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5546생성일: 2026년 10월 23일

(Z)-Tri-n-butyl(1-propenyl)tin → Diphenylmethyl 7-Phenoxyacetamido-3-(Z-1-propenyl)-3-cephem-4carboxylate

https://huagongshe.com/ko/reaction/5546

반응식

참여 물질

역할이름HCID투입량
반응물(Z)-Tri-n-butyl(1-propenyl)tinHCID 10914524—
반응물Diphenylmethyl 7-Phenoxyacetamido-3-[(fluorosulfonyl)oxy]-3-cephem-4-carboxylateHCID 88424184—
촉매palladium(II) acetateHCID 167845—
용매DichloromethaneHCID 6344—
생성물Diphenylmethyl 7-Phenoxyacetamido-3-(Z-1-propenyl)-3-cephem-4carboxylateHCID 1460894092.9%

반응 단계

A solution of palladium (II) acetate (3.6 mg, 0.016 mmole, 0.1 eq.) in dichloromethane (2 mL) was treated with Z-1-propenyl tri-n-butylstannane (66.2 mg, 0.2 mmole, 1.2 eq.) under an inert atmosphere and allowed to stir for 3 minutes. The resulting dark suspension was then treated with diphenylmethyl 7-phenoxyacetamido-3-[(fluorosulfonyl) oxy]-3-cephem-4-carboxylate (100.0 mg, 0.16 mmole, 1.0 eq.) in one portion and the reaction mixture was allowed to stir for 10 minutes. The reaction mixture was diluted with additional dichloromethane and washed with water (1×10 mL). The organic fraction was dried over magnesium sulfate and purified by flash filtration through a pad of silica gel (W. R. Grace, 951W) first with dichloromethane (50 mL) to remove the residual stannane and then with 10% ethyl acetate in dichloromethane (50 mL) which upon concentration furnished 80.4 mg (89%) of the title compound as a pale yellow solid. The product was then recrystallized from isopropyl alcohol to afford 62.3 mg (69%) of a white solid, mp. 103°-104° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05245027
출처 데이터셋uspto-grants-1993_09
ORD IDord-c2b21fff05b941f38cbaf9f020481d88
출처 메모uspto-grants-1993_09