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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354734생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/354734

반응식

참여 물질

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

반응 단계

To a stirred mixture of 2-(4-hydroxyphenyl)-3-methylbutyric acid (10.0 g; 0.0515 mol), dioxane (65 ml), sodium hydroxide (19.08 g, 18.56 g real; 0.464 mol), and water (30 ml) is bubbled chlorodifluoromethane (46 g; 0.532 mol) at 80° C. over a four-hour period. The reaction mixture is then poured into 250 ml of ice water, washed with ether, acidified with concentrated hydrochloric acid to pH 3, and extracted with 200 ml of ether. The ether extract is washed with 100 ml of water, dried with sodium sulfate, filtered, and evaporated to a white paste. A mixture of hexane and methylene chloride is added. The resulting mixture is filtered to remove the solid which is the starting material. The filtrate is evaporated to give 5.41 g of product as a clear brown oil. The product is at least 85% pure as calculated by NMR. NMR (CDCl3 -d5 pyridine): δ6.57 (t, J=74.3 Hz, 1 H); δ3.63 (s, imp.); δ3.25 (d, J=10 Hz, 1H); δ2.37 (m, 1H); δ1.19 (d, J=6.5 Hz, 3H); δ0.78 (d, J=6.5 Hz, 3H); δ13.82 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04377531
출처 데이터셋uspto-grants-1983_03
ORD IDord-28e4be6086394816853479cc99a1c62e
출처 메모uspto-grants-1983_03