HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373483Generated: October 26, 2026
Water → O-ethyl O-(2,2,3,3,4,4-hexafluorocyclopentyl) S-propyl thiophosphate
https://huagongshe.com/reaction/373483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | O-Ethyl S-propyl chlorothiophosphate | HCID 11745722 | — |
| Reactant | 2,2,3,3,4,4-Hexafluorocyclopentanol | HCID 19810485 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | O-ethyl O-(2,2,3,3,4,4-hexafluorocyclopentyl) S-propyl thiophosphate | HCID 21752582 | 22.2% |
Reaction Steps
4 g (0.02 mol) of 2,2,3,3,4,4-hexafluorocyclopentan-1-ol, dissolved in 50 ml of tetrahydrofuran, are treated, at -70° C., with 8 ml of a 2.5-molar butyllithium solution in hexane. The mixture is heated to -20° C. and 5 g (0.02 mol) of O-ethyl S-propyl chlorothiophosphate are then added dropwise. To complete the reaction, the mixture is stirred for 24 hours at 20° C., a little water is added to the reaction mixture, and the mixture is filtered through silica gel. After the solvent has been distilled off and the residue has been distilled, 1.6 g (22% of theory) of O-ethyl O-(2,2,3,3,4,4-hexafluorocyclopentyl) S-propyl thiophosphate of a boiling point of b.p.0.15 90°-92° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05164383 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-0ba86778f75946efa8f867fd53c1e25f |
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| Source note | uspto-grants-1992_11 |
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