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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233672생성일: 2026년 10월 25일

Benzyl Bromide → D-leucic acid benzyl ester

https://huagongshe.com/reaction/233672

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물TetrahydrofuranHCID 8028—
반응물(R)-2-hydroxy-4-methylpentanoic acidHCID 439960—
용매TriethylamineHCID 8471—
생성물D-leucic acid benzyl esterHCID 9991100—

반응 단계

To 150 ml of tetrahydrofurane of 14.50 of D-leucic acid, 15.2 g of triethylamine and then 14.4 ml of benzyl bromide are added, and the solution was stirred for 3 hours while refluxing. The insoluble matter produced from the reaction solution was filtered off, and the filtrate was concentrated in vacuo. The obtained residue was dissolved and extracted in 150 ml of ethyl acetate. The ethyl acetate layer was washed twice with saturated bicarbonate water, twice with 1N hydrochloric acid, and twice with saturated brine sequentially, and dried over sodium sulfate anhydride, and concentrated in vacuo. The obtained oily residue was dried, and the captioned compound was obtained. Yield: 18.34 g.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594006
출처 데이터셋uspto-grants-1997_01
ORD IDord-ec3d3fd529934f85b7a05b26f0e52b1d
출처 메모uspto-grants-1997_01