HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697554Generated: November 4, 2026
Water → 4-Fluoro-2-trifluoromethylbenzenethiol
https://huagongshe.com/reaction/1697554
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Fluoro-2-(trifluoromethyl)benzenesulfonyl Chloride | HCID 2737548 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Fluoro-2-trifluoromethylbenzenethiol | HCID 50998002 | 85% |
Reaction Steps
4-Fluoro-2-(trifluoromethyl)benzenesulphonyl chloride (2.0 g) was dissolved in dioxane (12 mL) under a N2-atmosphere at ambient temperature. Water (3.0 mL) and tris-(2-carboxylethyl)phosphine hydrochloride (8.73 g) was added afterwards. The reaction mixture is stirred under reflux for 6 h. The reaction mixture is cooled to 25° C. and dissolved with water (30 mL). The product is extracted with CH2Cl2 (100 mL) several times. The combined organic layers are washed with water and dried over Na2SO4. The organic layer is filtrated and evaporated to dryness to yield 1.27 g (85%) of a colorless liquid which is used without further purification. MS (ESI): m/z=194.9 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163793B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-70ace7d7a7c14a90af1d1ee56e3e8411 |
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| Source note | uspto-grants-2012_04 |
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