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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929622Generated: October 30, 2026

3-(4-(Trifluoromethyl)phenyl)propan-1-ol → 3-[4-(Trifluoromethyl)phenyl]propanal

https://huagongshe.com/reaction/1929622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-(Trifluoromethyl)phenyl)propan-1-olHCID 22443642—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Product3-[4-(Trifluoromethyl)phenyl]propanalHCID 21683807—

Reaction Steps

To an ice-cooled orange suspension of pyridinium chlorochromate (3.659 g; 16.896 mmol) in anhydrous DCM (20 ml) was added dropwise a solution of 3-(4-trifluoromethyl-phenyl)-propan-1-ol (2.300 g; 11.264 mmol) in anhydrous DCM (35 ml). The resulting black suspension was allowed to warm-up to rt and was stirred under nitrogen for 3 h. The reaction mixture was directly filtered over silicagel using DCM. After concentration to dryness under reduced pressure, the product 3-(4-trifluoromethyl-phenyl)-propionaldehyde was isolated as a pale yellow oil (1.970 g; 86.5%). LC-MS: tR=0.95 min.; [M+H]+: no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188082B2
Source datasetuspto-grants-2012_05
ORD IDord-5a230912feb04f9eb494536f1bf862fe
Source noteuspto-grants-2012_05