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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050044Generated: November 1, 2026

Methanol → (4-Bromo-3-fluorophenyl)methanol

https://huagongshe.com/reaction/1050044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-Bromo-3-fluorobenzaldehydeHCID 2783411—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product(4-Bromo-3-fluorophenyl)methanolHCID 2068229797%

Reaction Steps

To a solution of 4-bromo-3-fluorobenzaldehyde (10 g, 49.3 mmol) and NaBH4 (3.73 g, 99 mmol) in THF (100 mL) was added MeOH (100 mL) dropwise at 20° C. After LCMS analysis showed the starting material had disappeared, the solvent was removed in vacuo. The residue was dissolved in DCM (200 mL) and washed with H2O (60 mL) and brine (60 mL). The organic layer was dried over Na2SO4, filtered and concentrated to yield a white solid of (4-bromo-3-fluorophenyl)methanol (9.8 g, 47.7 mmol, 97.0% yield): 1H NMR (400 MHz, CD3OD) δ 7.54 (t, J=7.8 Hz, 1H), 7.18 (d, J=9.6 Hz, 1H), 7.06 (d, J=7.2 Hz, 1H), 4.56 (s, 2H); ES-LCMS m/z 188.9 (M−17).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382238B2
Source datasetuspto-grants-2016_07
ORD IDord-bf47c4c0d43346e4b0d7a818316e37ba
Source noteuspto-grants-2016_07