HuagongsheHuagongshe Chemistry Print Report · For research reference only
Caprolactam → 6-Oxohexanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | Methyl 6-oxohexanoate | HCID 81164 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Oxohexanoic acid | HCID 440918 | — |
Reaction Steps
A process for preparing ε-caprolactam is described in U.S. Pat. No. 4,730,040. In this process, methyl 5-formylvalerate is first hydrolyzed (step a) in the presence of water and an acidic agent to yield 5-formylvaleric acid. In this process, the 5-formylvaleric acid is reductively aminated in water through contact with ammonia and hydrogen using a ruthenium/zirconium on alumina catalyst, a Raney Nickel catalyst or a Raney Cobalt catalyst to obtain a 6-aminocaproic acid containing reaction mixture. After separation of ammonia, the reaction mixture obtained from the reductive amination is heated to 300° C. to form ε-caprolactam by cyclization of the 6-aminocaproic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06452002B2 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-7cb4340ed15c4f578086267a4bba5010 |
| Source note | uspto-grants-2002_09 |