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HRID 411831作成日:2026年10月27日

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

https://huagongshe.com/reaction/411831

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1,1-DimethoxyethaneHCID 10795—
反応物Potassium CarbonateHCID 11430—
反応物3,3-Dichloro-2-propenalHCID 17554—
反応物Cyclopropanecarboximidamide hydrochlorideHCID 2781916—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-Cyclopropyl-4-(3-trifluoromethylphenoxy)pyrimidineHCID 986049775%

反応手順

3,3-Dichloroacrolein (10 mmoles) diluted with dimethoxyethane (35 ml), is slowly added to a mixture consisting of a cyclopropylcarbamidine hydrochloride (10 mmoles), 3-trifluoromethylphenol (11 mmoles), potassium carbonate (40 rnmoles) and dimethyoxyethane (40 ml), which is stirred under reflux. When the addition of 3,3-dichloroacrolein is completed additional cyclopropylcarbamidine 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 2.1 g (75%) of the pure product having as a colorless liquid; 1H NMR (CDC13); δ=2.10 ppm (m, N═C(═N)═CH).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559307B2
出典データセットuspto-grants-2003_05
ORD IDord-1ec957835fbf4ea59e1c911d33f439c8
出典メモuspto-grants-2003_05