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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29281생성일: 2026년 10월 24일

Ethyl Acetate → methyl N-[(4'-nitro-1,1'-biphenyl-4-yl)sulfonyl]-L-valinate

https://huagongshe.com/ko/reaction/29281

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium BicarbonateHCID 516892—
반응물4-Nitrophenylboronic acidHCID 2773552—
반응물methyl N-[(4-bromophenyl)sulfonyl]-L-valinateHCID 47337186—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물methyl N-[(4'-nitro-1,1'-biphenyl-4-yl)sulfonyl]-L-valinateHCID 1006907781%

반응 단계

A mixture of 0.175 g (0.5 mmol) of methyl N-[(4-bromophenyl)sulfonyl]-L-valinate, 0.25 g (1.5 mmol) of 4-nitrophenylboronic acid, 0.087 g of tetrakis(triphenylphosphine)palladium and 8 mL of saturated sodium bicarbonate in 8 mL of ethylene glycol dimethyl ether were refluxed for 2 h, then cooled to room temperature. To the reaction was added 50 mL of ethyl acetate and 40 mL of water. The water layer was extracted with ethyl acetate. The combined ethyl acetate layers was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexane:ethyl acetate (2:1) to provide 0.159 g of methyl N-[(4′-nitro-1,1′-biphenyl-4-yl)sulfonyl]-L-valinate as a yellow solid. Yield 81%. m.p. 144-146° C.; MS: 391.0(M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0a555bc7f2294e2684f21f1665cd84dc
출처 메모uspto-grants-2008_09