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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 2-Fluoro-1-methoxy-5-methyl-3-(methylsulfinyl)benzene | HCID 89767693 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Fluoro-3-methoxy-5-methylbenzenethiol | HCID 89767672 | 51.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238639B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-ea7f7ee883d241b3b60d95f0f3c2670a |
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| Source note | uspto-grants-2016_01 |
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