Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 70467100 | HCID 70467100 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 70467132 | HCID 70467132 | 85.1% |
Reaction Steps
86.8 g of N-acetyl-2,2,4-trimethyltetrahydroquinoline are dissolved in 600 ml of acetic anhydride and the solution is cooled to 0° C. 28 g of fuming nitric acid in 50 ml of acetic anhydride are now added dropwise. The mixture is kept at 0° C. for a further 30 minutes and is then stirred overnight at room temperature. It is poured onto water and the precipitate is filtered off with suction. 89 g of 1-acetyl-2,2,4-trimethyl-6-nitrotetrahydroquinoline of melting point 91° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04600776 |
|---|
| Source dataset | uspto-grants-1986_07 |
|---|
| ORD ID | ord-ab0c223790b743809a0ab558d745deb1 |
|---|
| Source note | uspto-grants-1986_07 |
|---|