돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 579795생성일: 2026년 10월 26일

m-Chloroperbenzoic acid → 2-(Benzyloxy)-4-fluorophenol

https://huagongshe.com/reaction/579795

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물2,3-Dihydro-1,4-benzodioxin-6-yl isothiocyanateHCID 2776173—
반응물1-(2-(Benzyloxy)-4-fluorophenyl)ethanoneHCID 21241577—
용매DichloromethaneHCID 6344—
생성물2-(Benzyloxy)-4-fluorophenolHCID 2124158593%

반응 단계

A mixture of 11 parts of 1-[4-fluoro-2-(phenylmethoxy)phenyl]ethanone, 8.48 parts of 3-chlorobenzenecarboperoxoic acid and 260 parts of dichloromethane was stirred for 5 days at room temperature. The precipitate was filtered off and the filtrate was stirred in a saturate thiosulfurate solution for 15 minutes. The organic layer was separated and stirred in a saturate hydrogen carbonate solution for 15 minutes. The organic layer was separated, washed with water, dried, filtered and evaporated. The solid residue was stirred in 240 parts of methanol. 5.3 Parts of sodium methoxide were added portionwise. After complete addition, the whole was stirred for 1 hour at room temperature. After evaporation in vacuo at 50° C., the residue was stirred in water and acidified with a hydrochloric acid solution 3N. Trichloromethane was added, the organic layer was separated, washed twice with water, dried, filtered and evaporated, yielding 10 parts (93%) of 4-fluoro-2-(phenylmethoxy)phenol as a residue (intermediate 77).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04749702
출처 데이터셋uspto-grants-1988_06
ORD IDord-c1901a0ee32e49fea7b53722cf5f2cf7
출처 메모uspto-grants-1988_06