HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone Oxime → Laurolactam
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone Oxime | HCID 7517 | — |
| Reactant | Caprolactam | HCID 7768 | — |
| Reactant | Cyclododecanone, oxime | HCID 136762 | — |
| Product | Laurolactam | HCID 13690 | — |
Reaction Steps
An oxime can be converted into an amide compound by Beckmann rearrangement reaction, particularly an oxime derived from a cyclic ketone can be converted into a lactam. For example, cyclohexanone oxime gives ε-caprolactam which is a starting material for Nylon 6 and cyclododecanone oxime gives laurolactam which is a starting material for Nylon 12.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09376375B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-ed521d42fbe74f65b2239ad9b8c43268 |
| Source note | uspto-grants-2016_06 |