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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 235310생성일: 2026년 10월 25일

Trifluoroacetic acid → 3-(1-adamantyl)4-methoxy-N-(trifluoroacetyl)aniline

https://huagongshe.com/reaction/235310

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylamineHCID 8471—
반응물Ethyl chloroformateHCID 10928—
반응물Sodium AzideHCID 33557—
반응물Sodium BicarbonateHCID 516892—
반응물3-(1-Adamantyl)-4-methoxybenzoic acidHCID 5296503—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-(1-adamantyl)4-methoxy-N-(trifluoroacetyl)anilineHCID 1906828057%

반응 조건

온도0 °C

반응 단계

11.70 ml (84 mmol) of triethylamine in 10 ml of tetrahydrofuran and 8.70 ml (91 mmol) of ethyl chloroformate in 10 ml of tetrahydrofuran are successively added dropwise to a solution of 20.6 g (70 mmol) of 3-(1-adamantyl)-4-methoxybenzoic acid in 200 ml of tetrahydrofuran at 0° C. The reaction medium is stirred for 40 minutes at 0° C., 6.83 g (105 retool) of sodium azide, dissolved in 30 ml of water, are then added to this medium and the mixture is left stirring at 0° C. for 2 hours. The reaction medium is poured into ice-cold water, the mixture is extracted with dichloromethane and the organic phase is washed with water, dried over magnesium sulphate and evaporated. The residue is dissolved in 400 ml of dichloromethane, 7.3 ml (0.094 mol) of trifluoroacetic acid are added and the mixture is heated to reflux for 30 hours. The reaction medium is poured into saturated sodium bicarbonate solution and the organic phase is dried over magnesium sulphate and evaporated. The residue is chromatographed on silica with a dichloromethane/hexane (30:70) mixture to yield 14.1 g (57%) of 3-(1-adamantyl)-4-methoxy-N-(trifluoroacetyl)aniline, melting point 166°-167° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05597839
출처 데이터셋uspto-grants-1997_01
ORD IDord-c8dbc984b44b4365aa8244b736d5a392
출처 메모uspto-grants-1997_01