HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Imidazolidinone → 1-(N,N-diethylsulphamoyl)-2-oxo-tetrahydroimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Imidazolidinone | HCID 8453 | — |
| Reactant | N,N-diethylsulfamoyl chloride | HCID 11252267 | — |
| Product | 1-(N,N-diethylsulphamoyl)-2-oxo-tetrahydroimidazole | HCID 13031743 | — |
Reaction Steps
A mixture of 5.16 g of ethylene urea and 90 g of N,N-diethyl-sulphamoyl-chloride is heated at 110° for 3 hours. The reaction mixture is cooled and triturated with 300 ml of methanol, filtered and the filtrate evaporated off to dryness and the residue dissolved in 5% methanol in chloroform and chromatographed on a column of silica gel. That fraction which elutes with 5% methanol in chloroform is recrystallized from a mixture of methylenechlorid and hexane to give 1-(N,N-diethylsulphamoyl)--2-oxo-tetrahydroimidazole which melts at 80°-82°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976778 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-c6b434d8d7b146c5ab55a098aa3fda28 |
| Source note | uspto-grants-1976_08 |