HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine hydrochloride → O,O-diethyl N-(chlorothio)-n-propylphosphoramidothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | Sulfur dichloride | HCID 25353 | — |
| Reactant | O,O-diethyl propylphosphoramidothioate | HCID 2172696 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | O,O-diethyl N-(chlorothio)-n-propylphosphoramidothioate | HCID 20333951 | — |
Reaction Steps
A solution of 2.98 gm. (0.014 mole) O,O-diethyl n-propylphosphoramidothioate in 10 ml. hexane and 2 ml. triethylamine is added to a cold (0° C.) solution of 1.0 ml. (0.016 mole) sulfur dichloride in 10 ml. hexane slowly and with stirring. There is vigorous reaction and heavy precipitation of triethylamine hydrochloride. An additional 20 ml. hexane is added. The reaction mixture is kept at 0° to 5° C. and stirred for 30 minutes, then it is filtered. The filtrate is concentrated to a pale yellow oil by evaporating the hexane under reduced pressure. The oil comprises the desired O,O-diethyl N-(chlorothio)-n-propylphosphoramidothioate which can be used for further reactions with N-methylcarbamates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04208409 |
| Source dataset | uspto-grants-1980_06 |
| ORD ID | ord-eb62bfc35fec4a00bf1f1371c41c0480 |
| Source note | uspto-grants-1980_06 |