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HRID 242152作成日:2026年10月26日

Ethyl Acetate → (6-Chloropyridazin-3-yl)methanol

https://huagongshe.com/reaction/242152

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Thionyl ChlorideHCID 24386—
反応物Sodium borohydrideHCID 4311764—
反応物6-chloropyridazine-3-carboxylic AcidHCID 6415762—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物(6-Chloropyridazin-3-yl)methanolHCID 20557609—

反応条件

温度60 °C

反応手順

4.3 g (21.4 mmol) of 6-chloropyridazine-3-carboxylic acid are dissolved in 60 ml of dry toluene and heated to 60° C. At this temperature, 3.8 g (32.2 mmol) of thionyl chloride are added, and the mixture is stirred at this temperature for 3 h. The mixture is then heated at reflux for 4 h. After cooling to RT, the solvent is removed on a rotary evaporator. 20 ml of toluene are added, and the mixture is again evaporated to dryness. The residue is dissolved in 40 ml of methyl tert-butyl ether and cooled to 5° C. At this temperature, a solution of 1.7 g (47.2 mmol) of sodium borohydride in 37 ml of water is added dropwise. The mixture is stirred at RT for 20 h. 50 ml of ethyl acetate are then added, and the aqueous phase is extracted three times with in each case 10 ml of ethyl acetate. The combined organic phases are washed in each case twice with in each case 10 ml of sat. sodium bicarbonate solution and water. The solvent is removed on a rotary evaporator and the residue is purified chromatographically on silica gel 60 (mobile phase: gradient dichloromethane/ethanol 100:1→20:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653109B2
出典データセットuspto-grants-2014_02
ORD IDord-3fd82016978b4fd29e041774b9703100
出典メモuspto-grants-2014_02