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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58900생성일: 2026년 10월 25일

Benzyl Bromide → N-(tert-Butoxycarbonyl)-3,4-dibenzyloxyphenylalanine benzyl ester

https://huagongshe.com/reaction/58900

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물Potassium CarbonateHCID 11430—
반응물N-(tert-Buloxycarbonyl)-3,4-dihydroxy-L-phenylalanineHCID 14217229—
용매AcetonitrileHCID 6342—
생성물N-(tert-Butoxycarbonyl)-3,4-dibenzyloxyphenylalanine benzyl esterHCID 22976099163.3%

반응 조건

온도55 °C

반응 단계

K2CO3 (21.0 g, 150 mmol) was added to a solution of Boc-L-dopa (10.0 g, 33 mmol) in acetonitrile (100 mL) followed by addition of benzyl bromide (21.0 g, 123 mmol). The suspension was heated at 50-60° C. for 4 h and then cooled to ambient temperature. The mixture was filtered and the filtration cake was washed with acetonitrile (50 mL). The filtrate and washings were combined and concentrated to dryness. The residue was purified by flash column chromatography on silica gel (Hexane/EtOAc=20:1) to afford (S)-benzyl 3-(3,4-bis(benzyloxy)phenyl)-2-(tert-butoxycarbonylamino)propanoate (15.3 g, yield 80%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434761B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d81204e5ed364f4790ee10a56f8d230a
출처 메모uspto-grants-2016_09