HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → HCID 59620410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 44521548 | HCID 44521548 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 59620410 | HCID 59620410 | — |
Reaction Steps
Fuming nitric acid (2 mL) was added dropwise to acetic anhydride (81 mL) at an internal temperature of 8° C. or lower, and sulfuric acid (81 μL) and a solution of N-(2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)acetamide (8.1 g) in acetic acid (81 mL) were sequentially added thereto, followed by stirring at room temperature for 3.5 hours. Diisopropyl ether (162 mL) was added to the mixture, and stirring was performed under cooling on ice for 30 minutes. The formed precipitates were recovered through filtration, washed with diisopropyl ether, and dried under reduced pressure, whereby a mixture of the title compound (A) and N-(8-nitro-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)acetamide (B) (A:B=1:1) (7.15 g) was yielded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08501772B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-c3f3075abdb84194b9b664358ca0aecc |
| Source note | uspto-grants-2013_08 |