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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635249Generated: October 25, 2026

Phenethyl bromide → 1,5-Diphenylpentan-3-ol

https://huagongshe.com/reaction/635249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantBenzenepropanalHCID 7707—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product1,5-Diphenylpentan-3-olHCID 12838510—

Reaction Steps

A solution of 2-(bromoethyl)benzene (1.73 g; 9.33 mmol) in diethylether (10 mL) was added to a stirred slurry of magnesium turnings (250 mg; 10.18 mmol) in 5 mL of ether. The reaction was initiated with a heat gun, and after the addition was complete the mixture was heated on an oil bath for 30 minutes. 3-Phenyl-1-propanal (1.25 g; 9.33 mmol) was added in 10 mL of ether, and reflux was continued for 1 hour. The reaction was cooled and quenched with saturated ammonium chloride, extracted into 2x ethyl acetate, and the combined organic portions were dried and concentrated. Chromatographic purification on a silica gel column (10% ethyl acetate in hexane) delivered 1.42 g (63%) of the diphenyl alcohol. 1H NMR (300 MHz, CDCl3): δ1.84 (m, 4H); 2.61-2.76 (m,4H); 3.65 (m, 1H); 7.19-7.29 (m, 10H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187796B1
Source datasetuspto-grants-2001_02
ORD IDord-9897418fa5c541b1b709f2a38f9a17d4
Source noteuspto-grants-2001_02