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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186570Generated: November 2, 2026

1-Bromo-3,5-difluorobenzene → 5-((3,5-Difluorophenyl)(hydroxy)methyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/1186570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3,5-difluorobenzeneHCID 136313—
Reactant2-Fluoro-5-formylbenzonitrileHCID 2769582—
ReactantMagnesiumHCID 5462224—
SolventTetrahydrofuranHCID 8028—
Product5-((3,5-Difluorophenyl)(hydroxy)methyl)-2-fluorobenzonitrileHCID 6867156067.1%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a stirred suspension of magnesium turnings (2.6 g, 109 mmol) in anhydrous tetrahydrofuran under argon (10 mL), a solution of 1-bromo-3,5-difluoro-benzene (21 g, 109 mmol) in dry tetrahydrofuran (90 mL) was slowly added. The reaction mixture was stirred and heated at 90° C. until all magnesium was consumed (1 hour). Thereafter, the reaction was cooled at −10° C. and a solution of 2-fluoro-5-formyl-benzonitrile (13.5 g, 90.6 mmol) in 100 mL of anhydrous tetrahydrofuran was added during 30 min. After 1 hour, the reaction mixture was quenched by adding dropwise 200 mL of 20% ammonium chloride solution. Ethyl acetate was added, the layers were separated, and the aqueous layer was extracted twice with ethyl acetate. Organic layers were collected, washed with brine, dried and evaporated. Crude was triturated with isopropyl ether/hexane 1:1 (100 mL), filtered and washed with the same mixture (50 mL) to afford 16 gr of final product. Purification of the resulting organic phase by chromatography over silica gel (hexane/EtOAc 4:1) afforded 4.5 g of the title compound (total amount 20.5 g, 87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673893B2
Source datasetuspto-grants-2014_03
ORD IDord-e1e1890508764e65950942a8742c4582
Source noteuspto-grants-2014_03