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 | — |
| Catalyst | Nickel | HCID 935 | — |
| Catalyst | Cobalt | HCID 104730 | — |
| Product | 6-Aminohexanoic Acid | HCID 564 | — |
Reaction Steps
U.S. Pat. No. 4,730,040 uses methyl 5-formylvalerate as a starting material to produce caprolactam. In this process, methyl 5-formylvalerate is first hydrolyzed in the presence of an acidic catalyst at 30° to 200° C. to 5-formylvaleric acid, which is then reacted with excess ammonia and hydrogen in the presence of Raney nickel or Raney cobalt as a hydrogenation catalyst at 50° to 150° C. under superatmospheric pressure to form 6-aminocaproic acid. After the unreacted ammonia and hydrogen gas are removed, the aqueous mixture is heated to 150° to 370° C. under 100 bar to induce dehydrolyzation and cyclization of 6-aminocaproic acid to form caprolactam. Such process is very complicated and the yield is not high enough.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05977356 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-b29699f074a143508fbf77140ba15ba5 |
| Source note | uspto-grants-1999_11 |