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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1054739Generated: October 25, 2026

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

https://huagongshe.com/reaction/1054739

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 numberUS09394285B2
Source datasetuspto-grants-2016_07
ORD IDord-a43ab158e3014363b8dc7631e25448f1
Source noteuspto-grants-2016_07