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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385012Generated: October 29, 2026

N-bromobutanimide → 5-Bromo-2-hydroxy-3-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/385012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Hydroxy-3-(trifluoromethyl)benzaldehydeHCID 2779274—
SolventAcetonitrileHCID 6342—
Product5-Bromo-2-hydroxy-3-(trifluoromethyl)benzaldehydeHCID 277927876.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-hydroxy-3-trifluoromethylbenzaldehyde (59.16 g) was dissolved in acetonitrile (500 mL), and N-bromosuccinimide (57.56 g) was added to the solution, and then the mixture was stirred at 0° C. for 1 hour. The solvent was distilled off under reduced pressure and water was added, and then the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained crystal was washed with n-hexane (50 mL) to obtain the title compound (63.98 g) as a pale yellow crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367843B2
Source datasetuspto-grants-2013_02
ORD IDord-df56cfcacc9c41299ed5df619c12927b
Source noteuspto-grants-2013_02