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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591443Generated: November 1, 2026

Trifluoroacetic anhydride → 2-Fluoro-3-methoxy-5-methylbenzenethiol

https://huagongshe.com/reaction/591443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant2-Fluoro-1-methoxy-5-methyl-3-(methylsulfinyl)benzeneHCID 89767693—
SolventAcetonitrileHCID 6342—
Product2-Fluoro-3-methoxy-5-methylbenzenethiolHCID 8976767251.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 2-fluoro-1-methoxy-5-methyl-3-(methylsulfinyl)benzene (486 mg) and CH3CN (20 mL) was added TFAA (1.02 mL) at 0° C. The mixture was stirred at 0° C. for 1 h, and concentrated in vacuo. The residue was dissolved in a mixture of MeOH (3.5 mL) and TEA (3.5 mL) at 0° C. The solution was stirred at room temperature for 1 h, and concentrated in vacuo. The residue was diluted with saturated aqueous NH4Cl, and the mixture was extracted with EtOAc. The organic layer was extracted with 1N NaOH. The aqueous layer was acidified with 1N HCl and extracted with EtOAc. The combined organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo to give the title compound (214 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-ea7f7ee883d241b3b60d95f0f3c2670a
Source noteuspto-grants-2016_01