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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441049Generated: October 30, 2026

Hydrochloric Acid → p-(Trifluoromethoxy)benzaldehyde

https://huagongshe.com/reaction/1441049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant4-(Trifluoromethoxy)benzonitrileHCID 67621—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Productp-(Trifluoromethoxy)benzaldehydeHCID 69573—

Reaction Steps

Diisobutylaluminium hydride (11.8 ml. 1M solution in toluene) was added to a stirred solution of 4-cyanophenyl trifluoromethyl ether (2.0 g., Fairfield) in dry diethyl ether (100 ml.). The mixture was refluxed with stirring for 3 hours. The mixture was cooled and dioxane (5 ml.) containing water 1.0 ml.) was added. Dilute hydrochloric acid was added (60 ml. of 10% solution). The mixture was stirred for 30 minutes and extracted with diethyl ether. The ethereal extracts were washed with water and dried over anhydrous magnesium sulphate. The solvent was removed in vacuo and the residue was purified by chromatography on silica, eluting with 9:1 hexane:diethyl ether. 4-Trifluoromethoxybenzaldehyde was obtained as a colourless liquid (1.65 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502073
Source datasetuspto-grants-1996_03
ORD IDord-7c173880cb27470680db651cd27692ae
Source noteuspto-grants-1996_03