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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234490생성일: 2026년 10월 25일

Benzyl Bromide → Phenylmethyl 6-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoate

https://huagongshe.com/reaction/234490

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물6-((tert-Butoxycarbonyl)amino)hexanoic acidHCID 637602—
용매DichloromethaneHCID 6344—
생성물Phenylmethyl 6-[[(1,1-dimethylethoxy)carbonyl]amino]hexanoateHCID 12160267—

반응 단계

1.94 ml of DBU and then 1.54 ml of benzyl bromide are added at RT to a solution of 3 g of 6-(tert-butoxycarbonylamino)hexanoic acid in 60 ml of DCM and the mixture is stirred for 24 hours at RT. It is concentrated under vacuum, the residue is taken up with 100 ml of water and extracted with AcOEt, the organic phase is washed with a 5% solution of potassium carbonate, with a saturated solution of NaCl and with water and dried over sodium sulfate and the solvent is evaporated off under vacuum to give 2.8 g of the expected product, which is used as such.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594023
출처 데이터셋uspto-grants-1997_01
ORD IDord-f9b768c700394298bbbed1554bf678e4
출처 메모uspto-grants-1997_01