HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 6-Aminohexanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | 6-Oxohexanoic acid | HCID 440918 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Aminohexanoic Acid | HCID 564 | — |
Reaction Steps
Finally, DE-A-No. 3,602,377 discloses a process for preparing caprolactam wherein the 5-formylvaleric ester is initially hydrolyzed with water in the presence of a catalyst from 30° to 200° C. to 5-formylvaleric acid which is reacted with ammonia and hydrogen in the presence of a solvent and hydrogenation catalyst under a superatmospheric pressure at from 50° to 150° C. to give 6-aminocaproic acid, the ammonia and the catalyst are separated off, and the resulting solution of 6-aminocaproic acid is heated to 150°-370° C. to form caprolactam. For this process to be practised in industry, the yields must be improved. Moreover, this process requires an additional hydrolysis stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04963672 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-9ab972e368824a9cbcb1fc175c5b0394 |
| Source note | uspto-grants-1990_10 |