돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512808생성일: 2026년 10월 25일

Benzyl Chloride → Methyl 2-(benzyloxy)propanoate

https://huagongshe.com/reaction/512808

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물Methyl LactateHCID 11040—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
생성물Methyl 2-(benzyloxy)propanoateHCID 561764—

반응 단계

To a pre-cooled solution of potassium tertiary butoxide (538.4 g) in DMF (1750 ml) at −20 to −10° C., added racemic methyl lactate compound of formula-11 (500 g) followed by benzyl chloride (547 g) at −20 to −10° C. and the reaction mixture was stirred for 5 hours at the same temperature. After completion of the reaction, the reaction mixture was quenched with water and the reaction mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and 10% sodium chloride solution and then distilled off the solvent from ethyl acetate layer under reduced pressure to get the title compound as a residue. The obtained residue was taken into next step without isolation.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102664B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-36e5364bb8604b519f3405652f340859
출처 메모uspto-grants-2015_08