HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 3-Aminoazepan-2-one hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Lysine monohydrochloride | HCID 69568 | — |
| Solvent | 1-Hexanol | HCID 8103 | — |
| Product | 3-Aminoazepan-2-one hydrochloride | HCID 12228562 | 75% |
Reaction Steps
A stirred mixture of L-lysine hydrochloride 1 (55 g, 300 mmol) and NaOH (12 g, 300 mmol) in hexanol (1.2 L) is heated to reflux with a Dean-Stark trap used to remove H2O. The suspension is refluxed for 8 hours until all starting material is consumed (which maybe determined by 1H NMR). The suspension is then cooled and filtered to remove byproduct NaCl. The filtrate is concentrated and the resulting crude α-amino-ε-caprolactam 2 is dissolved in water. After acidification to pH 6 with addition of concentrated HCl and partial concentration, crystals maybe formed at room temperature to afford α-amino-ε-caprolactam hydrochloride (37 g) in 75% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367819B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-8b7c3e46c9f240828c8093af8d0f5bc0 |
| Source note | uspto-grants-2013_02 |