HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 54311612, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 54133889 | HCID 54133889 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 54311612 | HCID 54311612 | 16.2% |
Reaction Steps
A mixture of 5.3 g of 1-(2-chloroethyl)-1-nitroso-3-(2-propenyl)-3-(L-arabinopyranosyl)urea, 5.9 g of meta-chloroperbenzoic acid, 50 ml of methylene chloride and 50 ml of benzene is stirred at room temperature for 3 hours. After the reaction, the mixture is condensed under reduced pressure. The residue obtained is washed with ether and then purified by silica gel chromatography (Solvent: ethyl acetate). 0.9 g of 1-(2-chloroethyl)-1-nitroso-3-(oxiran-2-yl-methyl)-3-(L-arabinopyranosyl)urea is thereby obtained as yellow caramel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04241052 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-f7063c35a6c34d248fb55917ba3ae8a8 |
| Source note | uspto-grants-1980_12 |