HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → N-Acetoxyhexyl-1,2,3,4-tetrahydroquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-hydroxyhexyltetrahydroquinoline | HCID 67859558 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Acetoxyhexyl-1,2,3,4-tetrahydroquinoline | HCID 53737711 | — |
Reaction Steps
To a stirred solution of 233.4 g (1 mole) of N-hydroxyhexyltetrahydroquinoline and 153.1 g (1.5 moles) of acetic anhydride in dichloromethane are added 151.8 g (1.5 moles) of triethylamine and 8.5 g (1 mole %) of 4-N,N-dimethylaminopyridine, and the reaction is stirred at room temperature for 3 hours. The product solution is washed with cold 2N HCl followed by saturated sodium bicarbonate, and the organic layer is filtered through cotton and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05247042 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-bf199b56f7eb4319ac3c695eb26223f8 |
| Source note | uspto-grants-1993_09 |