HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Imidazolidinone → 1-Ethylsulphonyl-imidazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Imidazolidinone | HCID 8453 | — |
| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Product | 1-Ethylsulphonyl-imidazolidin-2-one | HCID 11286796 | — |
Reaction Steps
A mixture of 29.2g of ethyleneurea and 43.7 g of ethane sulphonyl chloride is heated at 110° for 3 hrs under nitrogen. The reaction mixture is triturated with 30 ml methanol and filtered. The filtrate is evaporated off and the residue is dissolved in chloroform and chromatographed on a column of 750 g of silica gel. The fraction which eluted with 5% methanol in chloroform, is recrystallized from a mixture of methylene chloride and hexane to afford 1-ethylsulphonyl-2-oxo-tetrahydroimidazole which melts at 114°-116°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976778 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-ad8cb015155e40c39c7c179f8277cc73 |
| Source note | uspto-grants-1976_08 |