HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 6-Aminohexanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methyl 6-oxohexanoate | HCID 81164 | — |
| Reactant | 6-Oxohexanoic acid | HCID 440918 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Aminohexanoic Acid | HCID 564 | — |
| Product | Caprolactam | HCID 7768 | — |
Reaction Steps
Such a process is described in U.S. Pat. No. 4,730,040. This patent publication describes a process in which first methyl 5-formylvalerate is hydrolysed in an aqueous medium to methanol and 5-formylvaleric acid. In a second step, the aqueous mixture obtained in the first step is contacted with ammonia and hydrogen in the presence of a hydrogenation catalyst. In this step 6-aminocaproic acid and a small amount of ε-caprolactam is obtained. The resulting aqueous mixture, which mixture will contain the methanol formed in the first step, is heated to a temperature between 150 and 370° C. at which temperature 6-aminocaproic acid reacts by cyclization to ε-caprolactam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05973143 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-61c86f08dd71490e913ccb0022c1daae |
| Source note | uspto-grants-1999_10 |