HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Amino-N-octyloxy-2,2,6,6-tetramethylpiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(1-Octyloxy-2,2,6,6-tetramethylpiperidin-4-yl)acetamide | HCID 23372128 | — |
| Product | 4-Amino-N-octyloxy-2,2,6,6-tetramethylpiperidine | HCID 23372093 | 82,592.398% |
Reaction Steps
A mixture of 40.0 grams (0.123 mmol) of N-(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl)acetamide and 6N hydrochloric acid is heated at reflux for three hours. The reaction mixture is cooled and extracted with 2×150 ml). The aqueous layer is made basic and extracted with 3:1 ether:dichloromethane (3×150 ml). The three organic extracts are combined, dried over anhydrous magnesium sulfate and then concentrated to an oil. Purification by Kugelrohr distillation at 110°-120° C./0.5 mm affords 28.9 grams (83% yield) of the title compound as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574162 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-2f465867ffa742f99f2d3f856983875b |
| Source note | uspto-grants-1996_11 |