HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 1-benzyl-2,3-dihydro-1H-imidazo[1,2-a]pyridinium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | HCID 23423819 | HCID 23423819 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-benzyl-2,3-dihydro-1H-imidazo[1,2-a]pyridinium bromide | HCID 86735012 | — |
Reaction Steps
To 2.0 g. of 2,3-dihydroimidazo[1,2-a]pyridine in 40 ml. of dry acetonitrile is added 3.42 g. of α-bromotoluene and the resulting mixture heated to reflux overnight. The solution is cooled to room temperature and treated with 30 ml. of diethyl ether. The precipitated solid is filtered and recrystallized from acetonitrile, 1.64 g., m.p. 143°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04129567 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-f6469acff457428c8841e7511c65bfd0 |
| Source note | uspto-grants-1978_12 |