Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178763Generated: October 30, 2026

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

https://huagongshe.com/reaction/2178763

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 numberUS09067921B2
Source datasetuspto-grants-2015_06
ORD IDord-8be073957a644c1fb553c8d7efeaf595
Source noteuspto-grants-2015_06