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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 372971생성일: 2026년 10월 24일

Tetramethylammonium Hydroxide Pentahydrate → (+/-)-alpha-tert.Butyloxycarbonylamino-3-(4'-chloro-5-(diethoxyphosphinyl)methyl-[1.1'-biphenyl]-3-yl) propanoic acid cinnamyl ester

https://huagongshe.com/ko/reaction/372971

반응식

참여 물질

역할이름HCID투입량
반응물Tetramethylammonium Hydroxide PentahydrateHCID 82620—
반응물BromomethylstyreneHCID 98116—
반응물HCID 14127515HCID 14127515—
용매DimethylformamideHCID 6228—
생성물(+/-)-alpha-tert.Butyloxycarbonylamino-3-(4'-chloro-5-(diethoxyphosphinyl)methyl-[1.1'-biphenyl]-3-yl) propanoic acid cinnamyl esterHCID 56990101—

반응 단계

To a solution of 1.05 g of the product of step b) in 5 ml dimethylformamide are added 362 mg tetramethylammonium hydroxide pentahydrate. The mixture is stirred at room temperature 1 1/2 hours and then treated with 394 mg cinnamyl bromide. The mixture is stirred at room temperature 17 hours. The mixture is diluted with ice/water (about 50 ml) and extracted with diethyl ether. The extracts are washed with 10 ml aqueous 1N KHCO3 solution, dried (Na2SO4) and evaporated to give the heading compound as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05162311
출처 데이터셋uspto-grants-1992_11
ORD IDord-01be88585a0243e0b188c3ce031ecad4
출처 메모uspto-grants-1992_11