HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697620Generated: October 31, 2026
Water → 4-Fluoro-2-trifluoromethylbenzenethiol
https://huagongshe.com/reaction/1697620
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 g) was dissolved in 1,4-dioxane (12 mL) and water (3 mL) under a nitrogen atmosphere. Tris-(2-carboxylethyl)phosphine hydrochloride (8.73 g) was added and the mixture was stirred under reflux for 6 h. The reaction mixture was cooled to 25° C. and water (20 mL) was added. The product was extracted 3 times with CH2Cl2 (20 mL). The combined organic layers were dried over Na2SO4 filtrated and evaporated to dryness to yield the title compound (1.27 g, 85%) as a colorless liquid. 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-726dc90012354925a2eb9970cd71a86d |
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| Source note | uspto-grants-2012_04 |
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