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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750476Generated: October 25, 2026

5-Bromo-2,4-dichloropyrimidine → (2,4-Dichloro-pyrimidin-5-yl)-(2,3-difluoro-6-methoxy-phenyl)-methanol

https://huagongshe.com/reaction/750476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
Reactant2,3-Difluoro-6-methoxybenzaldehydeHCID 2774112—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
Product(2,4-Dichloro-pyrimidin-5-yl)-(2,3-difluoro-6-methoxy-phenyl)-methanolHCID 21070646—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-bromo-2,4-dichloropyrimidine (Aldrich, 3.02 g, 13.25 mmol) in 20 mL of THF at −30° C., isopropyl magnesium chloride (Aldrich, 2M solution in THF, 7.12 mL, 13.25 mmol) was added dropwise and the mixture was stirred for 20 minutes. Then 2,3-difluoro-6-methoxy-benzaldehyde (Matrix, 2.28 g, 13.25 mmol) was added and the mixture was warmed to 0° C. and stirred for 40 minutes. The reaction was quenched with saturated ammonium chloride solution and the resulting mixture was extracted with EtOAc. The extract was dried with sodium sulfate. The solvent was removed on a rotary evaporator and the solid was treated with hexane (8 mL). The solid was filtered and dried to give an off-white solid. 3.42 g; Yield, 80.5%. MS (M+H)+, 322.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405220B2
Source datasetuspto-grants-2008_07
ORD IDord-9dcc2cfd066a499d8e93596560645710
Source noteuspto-grants-2008_07