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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076567Generated: October 30, 2026

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

https://huagongshe.com/reaction/1076567

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 three hours and then heated under reflux for about five 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 numberUS03957787
Source datasetuspto-grants-1976_05
ORD IDord-4bd4e5883c5c43638c896fc8a182dcf0
Source noteuspto-grants-1976_05