HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 5-(3-Amino-4-chlorophenyl)-5-hydroxy-1-methylpyrrolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-(3-Amino-4-chlorobenzoyl)propionic acid | HCID 14256802 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(3-Amino-4-chlorophenyl)-5-hydroxy-1-methylpyrrolidin-2-one | HCID 14256803 | — |
Reaction Steps
42.8 g of ethyl chloroformate are metered into a solution of 60 g of 4-(3-amino-4-chlorophenyl)-4-oxobutyric acid and 27.8 g of triethylamine in 500 ml of tetrahydrofuran in such a way that the temperature does not exceed 10° C. The mixture is stirred in the icebath for a further 10 min and then, while maintaining the cooling, a solution of 35 g of gaseous methylamine in 250 ml of tetrahydrofuran is added, during which a temperature of 25° C. should not be exceeded. After stirring for a further 45 minutes in the icebath, the solvent is removed by distillation, water is added to the residue, and the crystalline precipitate is filtered off. Crystals of melting point 154° C. (from ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04929643 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-8beb8b841f1c41acbc90ba7c0d4a88dc |
| Source note | uspto-grants-1990_05 |