HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → Bis [4-[(ethoxy)(propylthio)phosphoryloxy]phenyl]sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4,4'-Thiodiphenol | HCID 17570 | — |
| Reactant | Dicyclohexano-18-crown-6 | HCID 85955 | — |
| Reactant | O-Ethyl S-propyl chlorothiophosphate | HCID 11745722 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Bis [4-[(ethoxy)(propylthio)phosphoryloxy]phenyl]sulfide | HCID 13343963 | — |
Reaction Steps
To a 250 ml round bottom flask was added 4,4'-thiodiphenol (4.36 g, 20 mmol), O-ethyl S-n-propyl phosphorochloridothioate (9.12 g, 45 mmol), powdered potassium hydroxide (3.37 g, 60 mmol), dicyclohexano-18-crown-6 (catalytic quantity), and acetonitrile. This mixture was refluxed 14 hours, cooled to room temperature, and the organic soluble fraction decanted from the solids. The organic solution was diluted with ether and successively washed with 4M NaOH (3×100 ml), water (2×50 ml), 5% HCl (1×50 ml), water (2×50 ml), and brine (2×50 ml). After drying (MgSO4) the solution was concentrated under reduced pressure to give a colorless oil (4.8 g, 7.6 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04457922 |
| Source dataset | uspto-grants-1984_07 |
| ORD ID | ord-fc5b32dd410548f1b4fb89eab4fa1bc5 |
| Source note | uspto-grants-1984_07 |