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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447926생성일: 2026년 10월 27일

Chlorodifluoromethane → 4-(Difluoromethoxy)-alpha-(1-methylethyl)benzeneacetic acid

https://huagongshe.com/reaction/1447926

반응식

참여 물질

역할이름HCID투입량
반응물ChlorodifluoromethaneHCID 6372—
반응물Sodium HydroxideHCID 14798—
반응물1,4-DioxaneHCID 31275—
반응물2-(4-Hydroxyphenyl)-3-methylbutyric acidHCID 112192—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물4-(Difluoromethoxy)-alpha-(1-methylethyl)benzeneacetic acidHCID 1311856543%

반응 단계

Into an 80° C. magnetically stirred mixture of 10.00 g (0.0515 mol) of α-isopropyl-4-hydroxyphenylacetic acid, 65 ml of dioxane, 19.08 g (18.56 g real, 0.464 mol) of sodium hydroxide, and 30 ml of water is bubbled 46 g (0.532 mol) of chlorodifluoromethane over a period of 4 hours. The reaction mixture is poured into 250 ml of ice water and the resulting mixture is washed with ether, acidified with concentrated hydrochloric acid to pH 3, and then extracted with 200 ml of ether. The ether solution is washed once with 100 ml of water, dried with sodium sulfate, filtered, and then evaporated to give a white paste. A mixture of hexane and methylene chloride is added and the resulting mixture is filtered to remove the solid which is the starting material. The filtrate is evaporated to give 5.41 g of a clear brown oil. It is estimated that the product was at least 85% pure by nmr. NMR (CDCl3 -d5 pyridine), δ 7.43 (d, J=8.2 Hz, 2H), δ 7.08 (d, J=8.2 Hz, 2H), δ 6.57 (t, J=74.3 Hz, 1H), δ 3.63 (s, imp.), δ 3.25 (d, J=10 Hz, 1H), δ 2.37 (m, 1H), δ 1.19 (d, J=6.5 Hz, 3H), δ 0.78 (d, J=6.5 Hz, 3H), δ 13.82 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04178460
출처 데이터셋uspto-grants-1979_12
ORD IDord-bdaf1a3657914e7d8afb4104908e8e85
출처 메모uspto-grants-1979_12