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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1418787생성일: 2026년 10월 26일

Sodium hydride → N-benzyloxycarbonyl-3-[4-(1,4,7-trioxaoctyl)-phenyl]-alanine-methyl ester

https://huagongshe.com/reaction/1418787

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-Bromo-3,6-dioxaheptaneHCID 123532—
반응물Sodium BicarbonateHCID 516892—
반응물N-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl esterHCID 7010613—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
생성물N-benzyloxycarbonyl-3-[4-(1,4,7-trioxaoctyl)-phenyl]-alanine-methyl esterHCID 22940770—

반응 단계

6.59 g (20 mmol) of N-benzyloxycarbonyl-tyrosine-methyl ester is dissolved in 25 ml of anhydrous N,N-dimethylformamide and mixed at 0° C. under argon with 0.81 g (20.5 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 10 minutes, then 3.75 g (20.5 mmol) of 1-bromo-2-(2-methoxyethoxy)-ethane is added, the reaction temperature is allowed to increase to room temperature and stirred for another three hours. For working-up, the batch is taken up in toluene and shaken out several times against aqueous sodium bicarbonate solution. The organic phase is separated, dried on magnesium sulfate, filtered and concentrated by evaporation. The oily residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05885548
출처 데이터셋uspto-grants-1999_03
ORD IDord-1341ac2f27f648288d7130e58f5f5e93
출처 메모uspto-grants-1999_03