HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-carbomethoxy-N'-benzylsulfamoyl-O-methylisourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzylsulfamyl chloride | HCID 13529095 | — |
| Reactant | Methyl N-(iminomethoxymethyl)carbamate | HCID 137319931 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-carbomethoxy-N'-benzylsulfamoyl-O-methylisourea | HCID 70392213 | — |
Reaction Steps
A solution of benzylsulfamoyl chloride (168 g) in anhydrous THF (300 ml) is added dropwise to a stirred solution of N-carbomethoxy-O-methylisourea (107 g) and triethylamine (90 g) in anhydrous THF (800 ml) under nitrogen at -70° C. The resulting suspension is warmed to RT, filtered and the filtrate evaporated in vacuo. The residue is partitioned between methylene chloride and 0.5N aq. HCl. The organic layer is dried, filtered, and concentrated in vacuo affording the desired product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04704388 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-4099f6da5a8147cea0efd2977b40bde9 |
| Source note | uspto-grants-1987_11 |