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
An ε-caprolactam preparation process starting from methyl 5-formylvalerate is described in U.S. Pat. No. 4,730,040. In this process, methyl 5-formylvalerate is first hydrolyzed (step x) in the presence of water and an acidic agent to yield 5-formylvaleric acid. The acid is then further reacted (step y) in aqueous solvent with ammonia and hydrogen in the presence of a Raney nickel catalyst in one reaction step to yield 6-aminocaproic acid. After separation of ammonia, the aqueous mixture is heated to 300° C. (step z) to form ε-caprolactam by cyclization of the 6-aminocaproic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05717089 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-5ce1521905234053a7c3b2ef3959c6f6 |
| Source note | uspto-grants-1998_02 |