HuagongsheHuagongshe Chemistry Print Report · For research reference only
Monoisouron → N-[[[5-(1,1-Dimethylethyl)-3-isoxazolyl]amino]carbonyl]-N-methyl-1-butanesulfenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Monoisouron | HCID 186687 | — |
| Reactant | 1-butanesulfenyl chloride | HCID 10855449 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[[[5-(1,1-Dimethylethyl)-3-isoxazolyl]amino]carbonyl]-N-methyl-1-butanesulfenamide | HCID 20534529 | 10.9% |
Reaction Steps
To a solution of 1-methyl-3-(5-t-butyl-3-isoxazolyl)urea (1.97 g) in pyridine (30 ml), butylsulfenyl chloride (1.08 mol equivalent) is added at -30° to -40° C. The resultant mixture is allowed to stand at -30° to -40° C. for 6 hours and at room temperature overnight. The reaction mixture is chromatographed on a column of silica gel, whereby 1-methyl-1-butylthio-3-(5-t-butyl-3-isoxazolyl)urea (0.31 g) is obtained as an oil. I.R.: 1698, 1606 cm-1 (CCl4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04111680 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-b7a5e04cf53644888b3dfa7096e518ff |
| Source note | uspto-grants-1978_09 |