Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117956Generated: October 31, 2026

Water → 2-(3-Bromophenyl)ethan-1-ol

https://huagongshe.com/reaction/2117956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Sodium TartrateHCID 9357—
Reactant(3-Bromophenyl)acetic acidHCID 74653—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Bromophenyl)ethan-1-olHCID 2734090—

Reaction Steps

To a suspension of lithium aluminium hydride in dry tetrahydrofuran (50 ml) was added (3-bromophenyl)acetic acid (10 g) in tetrahydrofuran (100 ml) under ice cooling. The mixture was refluxed for 2 hurs. After cooling, to the reaction mixture were added water and aqueous Rochelle salt. The mixture was stirred for another 30 min. Aqueous layer was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and concentrated in vacuo to give 2-(3-bromophenyl)ethanol. This compound was used for the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442715B2
Source datasetuspto-grants-2008_10
ORD IDord-ed01c1f40fd5494eafb9f4ec23790caa
Source noteuspto-grants-2008_10