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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071091Generated: October 30, 2026

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

https://huagongshe.com/reaction/2071091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product3-Bromo-5-(trifluoromethyl)benzaldehydeHCID 16115438—

Reaction Steps

To 3-(trifluoromethyl)benzaldehyde (5 gm, 28.72 mmol) in sulfuric acid (13.5 ml) at 60° C., N-bromosuccinimide (6.13 g, 34.45 mmol) was added in 3 portions. After 2 h, the reaction mixture was cooled, diluted with cold water and filtered. Filter cake was washed with hexane. Volatiles were removed under reduced pressure and the crude residue of 3-bromo-5-(trifluoromethyl)benzaldehyde was carried to the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299267B2
Source datasetuspto-grants-2012_10
ORD IDord-55c9f391e93e4656902f23e6732ff89a
Source noteuspto-grants-2012_10