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HRID 1600125作成日:2026年10月26日

2,4-Difluorobenzaldehyde → 2,4-Difluoro-alpha-2-propenylbenzenemethanol

https://huagongshe.com/reaction/1600125

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DifluorobenzaldehydeHCID 73770—
反応物HCID 178455850HCID 178455850—
溶媒Diethyl EtherHCID 3283—
生成物2,4-Difluoro-alpha-2-propenylbenzenemethanolHCID 18924035—

反応条件

温度0 °C

反応手順

Under anhydrous condition at 0° C., a mixture of 18.0 g of freshly distilled 2,4-difluorobenzaldehyde and 120 ml of diethyl ether is treated,dropwise, with 139 ml of 1M allyl magnesium bromide. The reaction is stirred at 0° C. for 1 hour then slowly allowed to warm to room temperature. After 5 hours, thin layer chromatography indicates complete reaction. The mixture is cooled to 0° C. and quenched by the dropwise addition of 100 ml of ice cold saturated ammonium chloride. Two hundred ml of diethyl ether is added and the layers are separated. The aqueous layer is extracted with diethyl ether. The organic layers are combined, washed twice with saturated sodium chloride, dried , filtered and concentrated in vacuo. The residue is purified by Kugelrohr distillation (100° C.) to give 19.9 g of the desired product as a mixture of isomers.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05744465
出典データセットuspto-grants-1998_04
ORD IDord-bd1fe797e14145c891183eb03c251595
出典メモuspto-grants-1998_04