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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591559Generated: October 30, 2026

Anisole → 3-Fluoro-5-methoxybenzenethiol

https://huagongshe.com/reaction/591559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
Reactant1-Fluoro-3-methoxy-5-((4-methoxybenzyl)sulfanyl)benzeneHCID 89767862—
SolventTrifluoroacetic acidHCID 6422—
Product3-Fluoro-5-methoxybenzenethiolHCID 8976775265.3%

Reaction Steps

A mixture of anisole (12.04 g), 1-fluoro-3-methoxy-5-((4-methoxybenzyl)sulfanyl)benzene (6.2 g) and TFA (20 mL) was refluxed for 1 h, then concentrated in vacuo. Water was added to the residue and the mixture was extracted with EtOAc. The organic layer was washed with saturated aqueous NaHCO3 and extracted with 2N NaOH (100 mL×3). The water layer was acidified with 6N HCl and extracted with EtOAc. The EtOAc extract was washed successively with water and brine, dried over MgSO4, and concentrated in vacuo to give the title compound (2.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-2766f89b2e7a4cb69620e2cade1bf18f
Source noteuspto-grants-2016_01