Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871125Generated: October 30, 2026

3-Bromo-2-fluorobenzaldehyde → (3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanol

https://huagongshe.com/reaction/871125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-2-fluorobenzaldehydeHCID 22019361—
ReactantHCID 178418676HCID 178418676—
SolventTetrahydrofuranHCID 8028—
Product(3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanolHCID 86730390—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 3-bromo-2-fluorobenzaldehyde (0.150 g, 0.739 mmol) in THF (3.21 mL) cooled to −78° C. was added (4-fluorophenyl)magnesium bromide (0.443 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr, then allowed to warm to room temperature slowly over 2 hr. The reaction was quenched with a saturated aqueous solution of NH4Cl. The reaction mixture was diluted with CH2Cl2 and the layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). Organics were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a yellow residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969586B2
Source datasetuspto-grants-2015_03
ORD IDord-58e492eb32b1484eb7c606e467ec7abc
Source noteuspto-grants-2015_03