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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806839Generated: October 29, 2026

[3-Chloro-4-(trifluoromethyl)phenyl]methanol → 3-Chloro-4-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/1806839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-Chloro-4-(trifluoromethyl)phenyl]methanolHCID 44557937—
CatalystManganese dioxideHCID 14801—
Solvent1,2-DichloroethaneHCID 11—
Product3-Chloro-4-(trifluoromethyl)benzaldehydeHCID 1903128760%

Reaction Conditions

Temperature80 °C

Reaction Steps

Step A A mixture of 3-chloro-4-(trifluoromethyl)benzyl alcohol (Synquest) (4.77 g, 23 mmol) and activated MnO2 (19.5 g, 230 mmol) in 1,2-dichlorethane (80 mL) was heated and stirred at 80° C. for 3 h. The mixture was cooled to room temperature and filtered through a short pad of celite. The celite was washed with dichloromethane, and ethyl acetate. The filtrates were combined, concentrated, dried under reduced pressure to give 3-chloro-4-(trifluoromethyl)benzaldehyde as a light yellow oil (2.8 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-86b6bde40e0747a296759688ef21f51e
Source noteuspto-grants-2013_01