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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591427Generated: November 1, 2026

Trifluoroacetic acid → 2,5-Dichloro-3-methoxybenzenethiol

https://huagongshe.com/reaction/591427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
Reactant2,5-Dichloro-1-methoxy-3-((4-methoxybenzyl)sulfanyl)benzeneHCID 89767842—
SolventWaterHCID 962—
Product2,5-Dichloro-3-methoxybenzenethiolHCID 11865608967.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

The mixture of 2,5-dichloro-1-methoxy-3-((4-methoxybenzyl)sulfanyl)benzene (5.56 g) and anisole (9.18 mL) was added TFA (22.13 mL) at room temperature. The mixture was stirred at 80° C. for 20 min. After cooling, the mixture was diluted with water and extracted with EtOAc. The organic layer was extracted with 1N NaOH. The aqueous layer was acidified with 1N HCl, and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (2.38 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-e03f806d7cc8423dbeaf99ad107404bf
Source noteuspto-grants-2016_01