HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → O,S-dimethyl N-(N'-propoxycarbonyl-N'-isopropylaminosulfenyl)phosphoramidothioate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methamidophos | HCID 4096 | — |
| Reactant | Sulfur dichloride | HCID 25353 | — |
| Reactant | Pyridinium chloride | HCID 10176127 | — |
| Reactant | Propyl (chlorosulfenyl)(isopropyl)carbamate | HCID 12922683 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | O,S-dimethyl N-(N'-propoxycarbonyl-N'-isopropylaminosulfenyl)phosphoramidothioate | HCID 12922684 | — |
Reaction Steps
To a stirred mixture of 4.0 g (0.028 mol) O,S-dimethyl phosphoramidothioate, 2.2 g pyridine (0.028 mol) and 15 ml of anhydrous methylene chloride, chilled to 0°-5° C., was added dropwise 6.0 g (0.028 mol) propyl (chlorosulfenyl)(isopropyl)carbamate over a period of 15 minutes. Pyridine hydrochloride forms immediately during addition of the sulfenyl chloride. The reaction mixture was stirred for an additional half hour at room temperature after the addition of the sulfenyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04279897 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-c35fd00e208c42c198d6462c8173f4f0 |
| Source note | uspto-grants-1981_07 |