HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 136133141, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | N-Nitro-S-methylisothiourea | HCID 135927615 | — |
| Product | HCID 136133141 | HCID 136133141 | — |
Reaction Steps
The thus obtained crude oily substance was mixed with 3.07 g of S-methyl-N-nitroisothiourea, 0.1 g of dimethylaminopyridine (DMAP) and 30 ml of ethanol, and the mixture was refluxed. After the completion of reaction, ethyl acetate was added, and insolubles were then removed by filtration. The filtrate was concentrated under a reduced pressure to precipitate crystals, and the thus precipitated crystals were then removed by filtration. Next, the filtrate was concentrated under a reduced pressure to obtain an oily substance, and this oily substance was then purified by silica gel column chromatography (1:2 acetone/ethyl acetate) to obtain 1.04 g of 1-[(tetrahydro-3-furanyl)methyl]-2-(nitroimino)imidazolidine as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05614527 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-7eb93f9bb7d946b3aedc86a61ab64582 |
| Source note | uspto-grants-1997_03 |