戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 651730作成日:2026年10月26日

3-(Trifluoromethyl)phenol → 2-(4-Chlorophenyl)-4-(3-trifluoromethylphenoxy)pyrimidine

https://huagongshe.com/reaction/651730

反応式

関与物質

役割名称HCID仕込み量
反応物3-(Trifluoromethyl)phenolHCID 7376—
反応物Potassium CarbonateHCID 11430—
反応物3,3-Dichloro-2-propenalHCID 17554—
反応物4-Chlorobenzene-1-carboximidamide hydrochlorideHCID 203436—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-(4-Chlorophenyl)-4-(3-trifluoromethylphenoxy)pyrimidineHCID 986325480%

反応手順

3,3-Dichloroacrolein (10 mmoles) diluted with dimethoxyethane (35 ml), is slowly added to a mixture consisting of a 4-chlorobenzamidine hydrochloride (10 mmoles), 3-trifluoromethylphenol (11 mmoles), potassium carbonate (40 mmoles) and dimethoxyethane (40 ml), which is stirred under reflux. When the addition of 3,3-dichloroacrolein is completed additional 4chlorobenzamidine hydrochloride (1 mmoles) is added. The reaction mixture is stirred for 3 hours under reflux and subsequently cooled down to ambient temperature over night and filtered through silica. The organic phase is concentrated in vacuo. The residue was purified by chromatography on Al2O3 (petrol ethers/ethyl acetate: 20/1) to yield 2.79 g (80%) of the pure product having a melting point of 92° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06281358B1
出典データセットuspto-grants-2001_08
ORD IDord-f768b74fdf1545feb0499b9dc0950bd9
出典メモuspto-grants-2001_08