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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752868Generated: October 29, 2026

N-bromobutanimide → 3-Bromo-5-fluoro-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/1752868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-FluorosalicylaldehydeHCID 2737328—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-5-fluoro-2-hydroxybenzaldehydeHCID 2314895577.2%

Reaction Steps

N-bromosuccinimide (1.51 g, 8.52 mmol) was added to a magnetically stirred solution of 5-fluoro-2-hydroxybenzaldehyde (1 g, 7.1 mmol) in DMF (10 mL) and the mixture was stirred at room temperature for 5 hour. The mixture was diluted with ethyl acetate and the organic layer was washed with 5% citric acid, brine, dried over anhydrous sodium sulfate and concentrated by evaporation. Product was purified from the residue by chromatography over silica gel employing 50% ethyl acetate/hexanes to give 3-bromo-5-fluoro-2-hydroxybenzaldehyde (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09162986B2
Source datasetuspto-grants-2015_10
ORD IDord-ff3a9f0a48bd4479b6db57799e86359c
Source noteuspto-grants-2015_10