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HRID 865864作成日:2026年10月26日

4-Bromodiphenyl Ether → 1-(4-Phenoxyphenyl)prop-2-en-1-ol

https://huagongshe.com/reaction/865864

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromodiphenyl EtherHCID 7565—
反応物AcroleinHCID 7847—
反応物HCID 178418306HCID 178418306—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4-Phenoxyphenyl)prop-2-en-1-olHCID 1970581673%

反応条件

温度0 °C

反応手順

tert-Butyllithium (24.5 mL, 1.7M in pentane, 42.2 mmol) was added dropwise over 30 min to a solution of 4-bromodiphenyl ether (5.00 g, 20.1 mmol) in THF (50 mL) at -78° C. under argon. The cooling bath was removed and the bright yellow reaction mixture was warmed to 0° C. over 20 min. The reaction was stirred at 0° C. for 30 min, at which time a tan-colored solution developed. Freshly distilled acrolein (1.6 mL, 24 mmol) was added dropwise over 5 min. The colorless reaction mixture was stirred at 0° C. for 15 min, then quenched by addition of saturated NH4Cl (10 mL). The mixture was diluted with diethyl ether (200 mL) and the organic layer was washed with water (20 mL) and brine (50 mL), then dried over MgSO4. Evaporation gave a crude oil which was purified by flash chromatography on silica gel (400 g) eluted with a step gradient of 10:90 EtOAc/hexane to 15:85 EtOAc/hexane to 20:80 EtOAc/hexane to provide title compound (3.31 g, 73%) as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05567841
出典データセットuspto-grants-1996_10
ORD IDord-68936d09f9624790aeab8864ebd585c1
出典メモuspto-grants-1996_10