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HRID 537230作成日:2026年10月26日

Ammonium Chloride → 1-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethanol

https://huagongshe.com/reaction/537230

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物3,5-Dichloro-4-methylpyridineHCID 10953827—
反応物3-(Cyclopropylmethoxy)-4-(difluoromethoxy)benzaldehydeHCID 18973698—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物1-(3-Cyclopropylmethoxy-4-difluoromethoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethanolHCID 59443760—

反応条件

温度-30 °C

反応手順

A solution of 3-cyclopropylmethoxy-4-difluoromethoxy-benzaldehyde (5.00 g) and 3,5-dichloro-4-methylpyridine (2.57 g) in 50 ml dry THF was cooled to −30° C. Solid potassium t-butoxide (tBuOK, 1.96 g) was added portionwise maintaining the temperature between −30° C. and −20° C., thus obtaining a dark red solution. After completion of the addition, the mixture was stirred at −30° C. for 1 hour. A saturated aqueous solution of NH4Cl (50 ml) was then added to the reaction mixture, maintaining the temperature between −5° C. and −10° C. The color of the reaction mixture turned to yellow.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08859778B2
出典データセットuspto-grants-2014_10
ORD IDord-39dd1487f6f04c588c062b469444a3b4
出典メモuspto-grants-2014_10