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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406270Generated: October 30, 2026

2-Bromo-5-fluorobenzaldehyde → HCID 58140257, compound

https://huagongshe.com/reaction/1406270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-5-fluorobenzaldehydeHCID 2773321—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58140257HCID 5814025775.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-bromo-5-fluoro-benzaldehyde (17.0 g, 83.7 mmol) in tetrahydrofuran (100 mL), cooled to 0° C. under nitrogen, was added methyl magnesium chloride solution (3M in tetrahydrofuran, 31.0 mL, 93.0 mmol, 1.1 eq.) dropwise over a 20 min period. The resulting solution was stirred at 0° C. for 45 min before quenching with aqueous ammonium chloride solution (1M, 17 mL). The resulting mixture was partitioned between pentane (300 mL) and water (100 mL). The organic phase was washed with brine (50 mL) and then dried over magnesium sulphate. This mixture was filtered and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with a gradient of toluene in pentane (50:50 to 100:0 by volume) to produce the title compound as a colourless oil (13.8 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916593B2
Source datasetuspto-grants-2014_12
ORD IDord-60d25aaef0ac470b8a8a73fa7b27693f
Source noteuspto-grants-2014_12