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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662336Generated: October 29, 2026

4-Bromo-3-(butyloxy)benzoic acid → (4-Bromo-3-(butyloxy)phenyl)methanol

https://huagongshe.com/reaction/1662336

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-(butyloxy)benzoic acidHCID 57706230—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-3-(butyloxy)phenyl)methanolHCID 57705850102.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A solution of 20.1 (0.68 g, 2490 μmol) in THF (5 mL) was treated with borane THF complex (4979 μL, 4979 μmol) and stirred overnight at 65° C. The reaction mixture was quenched with MeOH, diluted with EtOAc, and washed with water and brine. The organic layer was dried over Na2SO4 and concentrated. The crude product was purified by combiflash (10 to 50% EtOAc/hexanes) yielding 20.2 (659.3 mg, 102% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-742b83af6866476c8c5c823506a9982a
Source noteuspto-grants-2011_10