HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → Caprolactam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Cyclohexanone Oxime | HCID 7517 | — |
| Product | Caprolactam | HCID 7768 | — |
| Product | Ammonium Sulfate | HCID 6097028 | — |
Reaction Steps
A precursor material for cyclohexanone oxime is cyclohexanone. Precursor materials for cyclohexanone can include cyclohexane, phenol, and benzene. Accordingly, the first step (or steps) in the production of ε-caprolactam is often a series of reductions and oxidations to form cyclohexanone from cyclohexane, phenol, or benzene. Cyclohexanone thus produced is next reacted with a hydroxylamine salt, usually the sulfate, to form cyclohexanone oxime and ammonium sulfate. The oxime is then rearranged in concentrated sulfuric acid, and the resulting lactam sulfate salt is hydrolyzed to form ε-caprolactam and additional ammonium sulfate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238804B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-6b01fd72482e4f7db6ca24d538f437af |
| Source note | uspto-grants-2007_07 |