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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414211Generated: November 1, 2026

Hydrochloric Acid → 2-(2-Bromophenyl)ethan-1-ol

https://huagongshe.com/reaction/1414211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantEthyl 2-(2-bromophenyl)acetateHCID 2780092—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
Product2-(2-Bromophenyl)ethan-1-olHCID 273408985.9%

Reaction Steps

To a stirred suspension of 106.0 g of lithium aluminum hydride in 3.7 l of anhydrous ether, is added, dropwise, a solution of 780.0 g of ethyl o-bromophenylacetate in 3.1 l of anhydrous ether. The reaction mixture is stirred for about 3 hours and then heated under reflux for about 5 hours. The mixture is cooled, then treated dropwise with 800 ml of water, and 1.5 l of 10% aqueous hydrochloric acid. The ether solution is washed, dried, concentrated, and the residue is distilled to give 554.0 g of o-bromophenethyl alcohol, bp. about 130°-132° (8mm), nD20 1,5760.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001233
Source datasetuspto-grants-1977_01
ORD IDord-6bae72c136d0493ab258c88403524551
Source noteuspto-grants-1977_01