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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247166Generated: October 29, 2026

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

https://huagongshe.com/reaction/2247166

Reaction equation

Participants

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

Reaction Conditions

Temperature210 °C

Reaction Steps

1-Methoxy-3-nitro-5-trifluoromethyl-benzene (10 g, Aldrich) and pyridine-HCl (41.8 g, Aldrich) were mixed together and heated neat at 210° C. in an open flask. After 2.5 h the mixture was cooled to RT and partitioned between 1N HCl and EtOAc. The EtOAc fraction was washed with 1N HCl (4×), brine (1×), dried with Na2SO4, filtered and concentrated in vacuo to form 3-nitro-5-trifluoromethyl-phenol as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687643B2
Source datasetuspto-grants-2010_03
ORD IDord-d21a37437d7f424fa5b6ac32152f0e8e
Source noteuspto-grants-2010_03