Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2779Generated: October 27, 2026

5-Bromo-2-fluorobenzaldehyde → (5-Bromo-2-fluorophenyl)methanol

https://huagongshe.com/reaction/2779

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-fluorobenzaldehydeHCID 736327—
ReactantSodium borohydrideHCID 4311764—
SolventTetrahydrofuranHCID 8028—
Product(5-Bromo-2-fluorophenyl)methanolHCID 277335297.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-bromo-2-fluoro-benzaldehyde (6.10 g, 30.0 mmol) in 30 mL of THF at 0° C. is added 5 mL of sodium borohydride (2.0M solution in triglyme, 10.0 mmol). The reaction mixture is stirred at 0° C. for 25 min and then quenched by the addition of 1N HCl. The mixture is diluted with EtOAc and the layers are separated. The organic layer is washed with H2O and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with 15% EtOAc/hexanes to afford the title compound (6.00 g, 29.3 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731315
Source datasetuspto-grants-1998_03
ORD IDord-dfa8e518af0e4946b9f86e5f4d0e8666
Source noteuspto-grants-1998_03