HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethyl N-(2-chloro-4-nitrophenyl)carbamate → 3-(2-Chloro-4-nitrophenyl)-2-oxazolidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethyl N-(2-chloro-4-nitrophenyl)carbamate | HCID 310713 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(2-Chloro-4-nitrophenyl)-2-oxazolidinone | HCID 23337318 | — |
Reaction Steps
A solution of 11.25 g of sodium methoxide in 50 ml of methanol was added drop-by-drop to a stirred solution of 58.0 g of 1A in 400 ml of ethanol. The mixture was refluxed for 5 minutes, then the volatile materials were evaporated under reduced pressure. The residue was treated with water and extracted with ether. The extract was dried and concentrated under reduced pressure. The residue was cooled and filtered to give 3-(2-chloro-4-nitrophenyl)-2-oxazolidinone (1B), as a white solid, mp: 94°-96° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04226612 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-0347dc0460dd46d2895dd2d891fb1b40 |
| Source note | uspto-grants-1980_10 |