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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871124Generated: October 26, 2026

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

https://huagongshe.com/reaction/871124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-2-fluorobenzaldehydeHCID 22019361—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product(3-Bromo-2-fluorophenyl)(phenyl)methanolHCID 71743205—

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 phenylmagnesium bromide (0.887 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr and then allowed to warm to room temperature slowly over 3 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 twice with CH2Cl2. The organic layers were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a colorless residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969586B2
Source datasetuspto-grants-2015_03
ORD IDord-cdc94b3ba03c4bd78911e3a632065075
Source noteuspto-grants-2015_03