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HRID 274029作成日:2026年10月25日

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

https://huagongshe.com/reaction/274029

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物TriethylamineHCID 8471—
反応物Ethyl chloroformateHCID 10928—
反応物Sodium AzideHCID 33557—
反応物Sodium BicarbonateHCID 516892—
反応物3-(1-Adamantyl)-4-methoxybenzoic acidHCID 5296503—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-(1-adamantyl)4-methoxy-N-(trifluoroacetyl)anilineHCID 1906828057%

反応条件

温度0 °C

反応手順

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 mmol) 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-admantyl)-4-methoxy-N-(trifluoroacetyl)aniline, melting point 166°-167° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387594
出典データセットuspto-grants-1995_02
ORD IDord-1091ac99025b48f6abcc0e3caed75091
出典メモuspto-grants-1995_02