HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484070Generated: October 30, 2026
Acetic Acid → 3-Methyl-1-(4-methoxyphenylcarbamoyl)-2-pyrrolidinone
https://huagongshe.com/reaction/484070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Isocyanato-4-methoxybenzene | HCID 79443 | — |
| Reactant | 3-Methylpyrrolidin-2-one | HCID 102848 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methyl-1-(4-methoxyphenylcarbamoyl)-2-pyrrolidinone | HCID 14881099 | 66% |
Reaction Steps
While 2 g of sodium hydride (60% oily) was being stirred in 50 ml of tetrahydrofuran, 5 g of 3-methyl-2-pyrrolidinone was added to the mixture, and the resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was cooled to not higher than 0° C., and 7.5 g of 4-methoxyphenyl isocyanate was added dropwise to the mixture, followed by stirring at the same temperature for 5 hours. Acetic acid was then added to the reaction mixture for neutralization, water was thereafter added to the mixture, and the solvent was distilled off in a vacuum. Water was added to the residue, and the precipitate was filtered off, giving 8.2 g of 3-methyl-1-(4-methoxyphenylcarbamoyl)-2-pyrrolidinone (yield 66%) having a melting point of 71° to 72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05229402 |
|---|
| Source dataset | uspto-grants-1993_07 |
|---|
| ORD ID | ord-f08f787b2cf7493baa7f6fe5b6f27cfd |
|---|
| Source note | uspto-grants-1993_07 |
|---|