HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Di-(2-ethylthioethyl)2-chloroethanephosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-(Ethylthio)ethanol | HCID 8075 | — |
| Reactant | (2-Chloroethyl)phosphonic dichloride | HCID 69645 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Di-(2-ethylthioethyl)2-chloroethanephosphonate | HCID 85916432 | — |
Reaction Steps
To a solution of 18.1 g (0.1 mol) of 2-chloroethane phosphonic acid dichloride in 150 ml of absolute ether is added dropwise with stirring a solution of 21.2 g (0.2 mol) of hydroxyethyl ethyl sulphide and 15.8 g of absolute pyridine in 100 ml of absolute ether at room temperature, during which the temperature increases to 35° and crystallisation occurs. Stirring is continued for a further 14 hours at 25° after which the crystals are removed by filtration and the ethereal filtrate is washed to neutrality with 5% hydrogen carbonate solution and water. It is dried and evaporated and further dried by rotation under high vacuum for 2 hours. A yellow oil is obtained having the following characterisation data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04190430 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-13e9384b72ff4f8c82a8c6f56f8594b2 |
| Source note | uspto-grants-1980_02 |