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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527467Generated: November 4, 2026

[3-Fluoro-2-(trifluoromethyl)pyridin-4-yl]methanol → 3-Fluoro-2-(trifluoromethyl)pyridine-4-carbaldehyde

https://huagongshe.com/reaction/1527467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[3-Fluoro-2-(trifluoromethyl)pyridin-4-yl]methanolHCID 68283421—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product3-Fluoro-2-(trifluoromethyl)pyridine-4-carbaldehydeHCID 86673864—

Reaction Steps

A mixture of (3-fluoro-2-trifluoromethyl-pyridin-4-yl)-methanol (0.620 g, 3.18 mmol) and activated MnO2 (3.20 g, 36.5 mmol) in CH2Cl2 was stirred at RT overnight. The solid was filtered off, washed with CH2Cl2, and the filtrate was concentrated under mildly reduced pressure to afford the title compound as a yellow liquid. MS (LC/MS): 212.0 [M+NH4]+, 226.0 [M+MeOH]+. tR (HPLC conditions c): 3.26 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-8b86983cf75a440fb942803377df3f4b
Source noteuspto-grants-2015_07