HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741805Generated: October 31, 2026
Water → 5-Fluoro-3-(hexafluoro-2-hydroxyprop-2-yl)thiophenol
https://huagongshe.com/reaction/741805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 5-Fluoro-3-(hexafluoro-2-hydroxyprop-2-yl)-1-(2-trimethylsilylethylthio)benzene | HCID 19426956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Fluoro-3-(hexafluoro-2-hydroxyprop-2-yl)thiophenol | HCID 19426933 | 44.2% |
Reaction Steps
To a solution of 5-fluoro-3-(hexafluoro-2-hydroxyprop-2-yl)-1-(2-trimethylsilylethylthio)benzene (1 g, 2.54 mmol Step 2) in dry DMF (20 mL) was added tetrabutylammonium fluoride (1M in THF) (Aldrich) (6.4 mL, 6.4 mmol) and the reaction mixture was heated at 60° C. for 30 min.. The reaction mixture was then added to H2O and extracted with EtOAc. The combined organic phase were washed with brine, dried and evaporated to give a residue which was chromatographed on silica gel eluting with 8:2 mixture of hexane:EtOAc to afford the title compound (330 mg, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05552437 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-c4d6d27dd8124dea9bea9e788ed25b94 |
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| Source note | uspto-grants-1996_09 |
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