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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | 2,5-Dichloro-1-methoxy-3-((4-methoxybenzyl)sulfanyl)benzene | HCID 89767842 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,5-Dichloro-3-methoxybenzenethiol | HCID 118656089 | 67.4% |
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
| 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-e03f806d7cc8423dbeaf99ad107404bf |
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| Source note | uspto-grants-2016_01 |
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