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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1088877생성일: 2026년 10월 27일

Ammonia → 2-Methoxy-6-(trifluoromethyl)phenol

https://huagongshe.com/reaction/1088877

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Trimethyl borateHCID 8470—
반응물3-(Trifluoromethyl)anisoleHCID 96691—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매N,N,N',N'-TetramethylethylenediamineHCID 8037—
용매HexaneHCID 8058—
생성물2-Methoxy-6-(trifluoromethyl)phenolHCID 15133336—

반응 조건

온도-78 °C

반응 단계

A solution containing 160 ml of 1.6 molar butyllithium in hexane, 300 ml of tetrahydrofuran and 40 ml of N,N,N',N'-tetramethylethylenediamine was cooled to -78° C. and 43.3 g of 3-trifluoromethylanisole was added with stirring under nitrogen atmosphere. The solution was allowed to warm up to room temperature and cooled then again to -78° C. after which 35 ml of trimethyl borate was added. The solution was warmed up to 20° C. and 50 ml of conc. ammonia solution was added. The solvents were evaporated in reduced pressure and to the residue 60 ml of 98-100% formic acid followed with 25 ml of 35% hydrogen peroxide were added. The solution was extracted with ether-petroleum ether (1:1). The organic phase was separated and the product was extracted with 2.5 N NaOH-solution. The aqueous phase was acidified with hydrochloric acid and the product was extracted in dichloromethane. The solvent was removed for the most part in vacuo after which petroleum ether was added. The crystalline product was filtered, yield 8.5 g (18%), m.p. 51°-53° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04963590
출처 데이터셋uspto-grants-1990_10
ORD IDord-5da80404712f44faa90d7573ab8ce473
출처 메모uspto-grants-1990_10