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HRID 129807作成日:2026年10月24日

3-Hydroxybenzaldehyde → 3-(1-Propenyl)phenol

https://huagongshe.com/ja/reaction/129807

反応式

関与物質

役割名称HCID仕込み量
反応物3-HydroxybenzaldehydeHCID 101—
反応物Diethyl EtherHCID 3283—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
触媒Phosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
溶媒TetrahydrofuranHCID 8028—
生成物3-(1-Propenyl)phenolHCID 5395934093%

反応条件

温度0 °C

反応手順

To a suspension of (ethyl)triphenylphosphonium bromide (35 g, 94.3 mmol) in THF (95 mL) was added potassium bis (trimethylsilyl)amide (180 ml, 0.5M in toluene, 90.2 mmol) dropwise. The reaction was stirred at 0° C. for 30 min, then a solution of 3-hydroxy-benzaldehyde (5 g, 41.0 mmol) in THF (5 mL) was added dropwise. After addition the reaction was stirred at 0° C. for 1 h. Ethyl ether (200 mL) was added to dilute the reaction. The organic layer was washed with water (50 mL×2), brine (50 mL×2) and dried over magnesium sulfate. Purification was performed by flash chromatography on 600 g silica gel, loaded and eluted with 10% ethyl acetate in hexane. Pure fractions were combined and evaporated to give the title compound (5.1 g, 93%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05470845
出典データセットuspto-grants-1995_11
ORD IDord-e85e3f0ca5084a3fbcd0a85b8b987a7b
出典メモuspto-grants-1995_11