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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361603Generated: October 30, 2026

3-Methoxy-5-nitrobenzotrifluoride → 3-Hydroxy-5-nitrobenzotrifluoride

https://huagongshe.com/reaction/1361603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxy-5-nitrobenzotrifluorideHCID 520597—
ReactantPyridinium chlorideHCID 10176127—
SolventDichloromethaneHCID 6344—
Product3-Hydroxy-5-nitrobenzotrifluorideHCID 2756251—

Reaction Conditions

Temperature200 °C

Reaction Steps

To a solution of 1-methoxy-3-nitro-5-(trifluoromethyl)benzene (1.0 g, 4,5 mmol) in dichloromethane (10 ml) was added pyridine hydrochloride salt (4.0 g, 35 mmol). After addition dichloromethane was removed under vacuum and the resulting solid mixture was heated at 200° C. overnight in an open reaction flask. After cooling to RT, 10% HCl (50 ml) was added and the mixture was extracted with EtOAc (3×50 ml). The combined organic layer was washed with brine (50 ml) and dried over Na2SO4. Solvent was removed under vacuum and the residue was purified by flash column chromatography on the silica gel (hexane/EtOAc=3:1) to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880000B2
Source datasetuspto-grants-2011_02
ORD IDord-eaf4e0c21fc74c92a586daf6d58ed2ed
Source noteuspto-grants-2011_02