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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244902Generated: October 31, 2026

Hydrochloric Acid → 2-Bromo-5-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/2244902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
Reactant2-Bromo-5-(trifluoromethyl)benzonitrileHCID 12223980—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product2-Bromo-5-(trifluoromethyl)benzaldehydeHCID 7018047—

Reaction Steps

To a solution of 2-bromo-5-(trifluoromethyl)benzonitrile (10.0 g, 40 mmol) in dichloromethane (100 mL) was dropwise added a 1.0 M solution of diisobutylaluminum hydride in hexane (48 mL). The resulting solution was stirred under nitrogen at ambient temperature for 1 h and was then diluted by addition of ether (100 mL). After cooling in an ice bath, a 3 N solution of HCl was carefully added, and the mixture was vigorously stirred at ambient temperature for 15 min. The organic layer was washed with brine, dried (MgSO4) and evaporated. The resulting oil was purified by flash chromatography (5% EtOAc/hexane) affording 5 g of 2-bromo-5-trifluoromethylbenzaldehyde. 1H NMR (CDCl3) δ 10.39 (s, 1H), 8.18 (d, J=2 Hz, 1H), 7.82 (d, J=8.8 Hz, 1H), 7.70 (dd, J=8.5 Hz, 2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678798B2
Source datasetuspto-grants-2010_03
ORD IDord-6b38b964226a465880e2c59f9e87cbca
Source noteuspto-grants-2010_03