Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25856Generated: October 25, 2026

Hydrochloric Acid → 1-Benzyl-3-bromobenzene

https://huagongshe.com/reaction/25856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(3-Bromophenyl)(phenyl)methanolHCID 285827—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventDimethoxyethane ethanolHCID 20074477—
SolventDiethyl ether methanolHCID 21864698—
Product1-Benzyl-3-bromobenzeneHCID 59753271.17%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 422 mg (11.12 mmol, 1.31 eq.) lithium aluminum hydride in 30 ml dry ether a solution of 1.38 g (10.35 mmol, 1.22 eq.) aluminum chloride in 18 ml dry ether was added cautiously under stirring. After the complete addition the resulting mixture was stirred for 30 min at r.t. before a solution of 2.24 g (8.52 mmol) (3-Bromo-phenyl)-phenyl-methanol (prepared above) in 19 ml dry ether was added dropwise. Then the mixture was refluxed for 12 h and after that cooled to 0° C. in an ice-bath. After adding cautiously 10 ml of a mixture of ether/methanol (1:1) 28 ml 1 N HCl-solution was added and the mixture was extracted with ether. The comb. org. fractions were washed with brine, dried over Na2SO4 and evaporated. Column chromatography (PE/CH2Cl2 (9+1)) yielded 1.50 g (6.06 mmol, 71.17%) 1-Benzyl-3-bromo-benzene (87) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858600B2
Source datasetuspto-grants-2005_02
ORD IDord-2498bafd8b25431aa75a2efba08ee720
Source noteuspto-grants-2005_02