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HRID 1388947作成日:2026年10月25日

Hydrochloric Acid → (4-Difluoromethoxyphenyl)(cyclopropyl) ketone

https://huagongshe.com/reaction/1388947

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Diethyl EtherHCID 3283—
反応物BromocyclopropaneHCID 78037—
反応物4-(Difluoromethoxy)benzonitrileHCID 2736990—
反応物MagnesiumHCID 5462224—
溶媒TetrahydrofuranHCID 8028—
生成物(4-Difluoromethoxyphenyl)(cyclopropyl) ketoneHCID 20469192—

反応手順

Upon a dry argon atmosphere, a mixture of 1.6 g (0.066 mole) of magnesium, 7.9 g (0.066 mole) of cyclopropylbromide, 60 ml of anhydrous diethyl ether, and 60 ml of anhydrous tetrahydrofuran was heated at reflux for 2.5 hours. The stirred mixture was cooled to room temperature, and a solution of 11.1 g (0.066 mole) of (4-difluoromethoxybenzonitrile) in 40 ml of anhydrous diethyl ether and 40 ml of anhydrous tetrahydrofuran was added during one hour. After complete addition, the mixture was heated at reflux for two hours, then stirred at room temperature for approximately 18 hours. A 100 ml portion of 2 N hydrochloric acid was added slowly to the mixture, and the whole was stirred for one hour. The mixture was extracted with three 100 ml portions of diethyl ether. The ether extracts were combined, dried over anhydrous magnesium sulfate and filtered. The filtrate was evaporated under reduced pressure to give an oil. The oil was subjected to column chromatography on silica gel, eluting with toluene/ethyl acetate (95:5), to give 8.3 g of (4-difluoromethoxyphenyl)(cyclopropyl) ketone.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04434182
出典データセットuspto-grants-1984_02
ORD IDord-caeb65ea2cd242219019afdfdc16f935
出典メモuspto-grants-1984_02