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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129791Generated: October 25, 2026

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

https://huagongshe.com/reaction/129791

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromodiphenyl EtherHCID 7565—
ReactantAcroleinHCID 7847—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Phenoxyphenyl)prop-2-en-1-olHCID 1970581673%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05470845
Source datasetuspto-grants-1995_11
ORD IDord-998384099d33431ba1faea82a60631df
Source noteuspto-grants-1995_11