HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 6-Bromo-3-nitroimidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-Bromoimidazo[1,2-a]pyridine | HCID 2795547 | — |
| Product | 6-Bromo-3-nitroimidazo[1,2-a]pyridine | HCID 28875888 | — |
Reaction Steps
A solution of 24 gms. (0.122 mole) of 6-bromoimidazo [1,2-a] pyridine in 80 ml. of concentrated sulfuric acid is treated dropwise with 24 ml. of concentrated nitric acid while maintaining a temperature of 15° C. with external cooling. When the addition is complete, the reaction mixture is stirred at room temperature for 1/2 hour and poured onto 450 gm. of ice. The pH of the mixture is adjusted to pH 4 with aqueous potassium hydroxide and the resultant solids are collected by filtration. The filter cake is washed with water and dried. Recrystallization from methylene chloride-hexane yields pure 3-nitro 6-bromoimidazo [1,2-a] pyridine m.p. 160°-161° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04146642 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-06caeeee2e464de998da9acc60a5625a |
| Source note | uspto-grants-1979_03 |