Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Bromo-6-fluoro-2-methyl-1,2,3,4-tetrahydroquinoline | HCID 12896817 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | HCID 13577653 | HCID 13577653 | — |
Reaction Steps
To 6.0 g of 5-bromo-6-fluoro-1,2,3,4-tetrahydroquinaldine was added 50 ml of acetic anhydride and one drop of concentrated sulfuric acid. The solution was heated on a steam bath for two hours, then cooled to about 20° C. The solution was basified with 10% sodium hydroxide solution. The solution was extracted with chloroform, and the chloroform extracts were evaporated to provide an oil which was distilled in vacuo to provide N-acetyl-5-bromo-6-fluoro-1,2,3,4-tetrahydroquinaldine. The structural assignment was supported by nuclear magnetic resonance spectral analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04472407 |
|---|
| Source dataset | uspto-grants-1984_09 |
|---|
| ORD ID | ord-e7494964c2a0408bb219209964f9baf6 |
|---|
| Source note | uspto-grants-1984_09 |
|---|