Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | S-Propyl phosphorodichloridothioate | HCID 12941235 | — |
| Reactant | 2,2,3,3,4,4-Hexafluorocyclopentanol | HCID 19810485 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 56981933 | HCID 56981933 | 27% |
Reaction Steps
20 g (0.1 mol) of S-propyl dichlorothiophosphate are dissolved in 500 ml of hexane, and the solution is first treated, between 0° and -5° C., with 20 ml (0.14 mol) of triethylamine and then with 20 g (0.1 mol) of 2,2,3,3,4,4-hexafluorocyclopentan-1-ol, dissolved in 50 ml of methylene chloride. The mixture is stirred for 2 hours at 20° C., and ammonia is then passed in at 20° C. (DC check). To complete the reaction, the mixture is stirred for 24 hours at 20° C., the solid is filtered off, and the solvent is distilled off under reduced pressure. The residue is then purified further by filtration through silica gel (cyclohexane:ethyl acetate=7:3 parts by volume). After the solvent has been distilled off, 8.6 g (27% of theory) of O-(2,2,3,3,4,4-hexafluorocyclopentyl) S-propyl thiophosphoramidate of refractive index nD20 =1.4390 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-5a3eef971b734a838e0cbc9455981134 |
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| Source note | uspto-grants-1992_11 |
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