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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1418790생성일: 2026년 10월 27일

1-Bromopropane → N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester

https://huagongshe.com/reaction/1418790

반응식

참여 물질

역할이름HCID투입량
반응물1-BromopropaneHCID 7840—
반응물Sodium hydrideHCID 24758—
반응물Sodium BicarbonateHCID 516892—
반응물N-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl esterHCID 7010613—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl esterHCID 22940772—

반응 단계

4.94 g (15 mmol) of N-benzyloxycarbonyl-tyrosine-methyl ester is dissolved in 25 ml of anhydrous N,N-dimethylformamide and mixed at 5° C. under argon with 0.61 g (15.5 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 10 minutes, then 1.91 g (15.5 mmol) of propyl bromide is added, the reaction temperature is allowed to increase to room temperature and it is stirred for another two hours. For working-up, the batch is taken up in ethyl acetate 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 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-1b1b6d4e4479430986678588eb86f835
출처 메모uspto-grants-1999_03