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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465864Generated: October 29, 2026

3-Bromobenzoic acid → 3-Bromobenzyl alcohol

https://huagongshe.com/reaction/465864

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromobenzoic acidHCID 11456—
SolventTetrahydrofuranHCID 8028—
Product3-Bromobenzyl alcoholHCID 85141—

Reaction Steps

To a solution of 50.0 g (0.25 mols, Aldrich) of 3-bromobenzoic acid in 100 ml of dry tetrahydrofuran (THF) cooled to 0° is added slowly 100 ml (1.0M in THF, 100 mmols, Aldrich) of borane-tetrahydrofuran complex. The reaction is stirred at 0° for 1 hour then at room temperature for 18 hours. The reaction is quenched by dropwise addition of water then concentrated in vacuo to remove solvent. The residue is partitioned between diethyl ether and 1M aqueous HCl. The organic layer is separated, washed with 1M aqueous sodium hydroxide, brine, dried (magnesium sulfate) and concentrated in vacuo to afford title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05153327
Source datasetuspto-grants-1992_10
ORD IDord-52210bfb74a542e19ea8b7fd8f2c9e76
Source noteuspto-grants-1992_10