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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338396Generated: October 26, 2026

1-(4-Bromophenyl)cyclobutane-1-carboxylic acid → (1-(4-Bromophenyl)cyclobutyl)methanol

https://huagongshe.com/reaction/338396

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)cyclobutane-1-carboxylic acidHCID 16769919—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product(1-(4-Bromophenyl)cyclobutyl)methanolHCID 5853868962%

Reaction Steps

To a solution of 1-(4-bromophenyl)cyclobutanecarboxylic acid (300 mg, 1.20 mmol) in 1,4-dioxane (5 mL) was added borane dimethylsulfide complex (0.24 mL, 2.4 mmol) dropwise at 0° C. The ice bath was removed, and the reaction mixture was stirred at room temperature for 10 min. The reaction mixture was quenched with methanol (20 mL). The organic solvents were removed under reduced pressure to give a residue, which was dissolved in ethyl acetate, then washed with brine. The organic phase was concentrated to give [1-(4-bromophenyl)cyclobutyl]methanol (170 mg, 62% yield) as a yellow oil which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-02cdec2d774246288b2abeba53c2dde3
Source noteuspto-grants-2014_11