Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806864Generated: November 1, 2026

beta-Phenylisovaleric acid → 3-Methyl-3-phenylbutan-1-ol

https://huagongshe.com/reaction/1806864

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbeta-Phenylisovaleric acidHCID 13890—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-3-phenylbutan-1-olHCID 232460100%

Reaction Steps

Step A To a solution of 3-methyl-3-phenylbutanoic acid (ChemBridge) (4.46 g, 25 mmol) in anhydrous tetrahydrofuran (150 mL) at 0° C. was added a tetrahydrofuran solution (1 M) of BH3.THF (Aldrich, 50 mL, 50 mmol) under nitrogen. The reaction mixture was stirred at room temperature for 3 h, then concentrated. The residue was partitioned between ethyl acetate and water. The organic layer were separated, washed with water, aqueous HCl solution, brine, dried over MgSO4, and concentrated to give 3-methyl-3-phenyl-butan-1-ol as a colorless oil (4.1 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-869db1525e3f49b08d3e50649ad39717
Source noteuspto-grants-2013_01