HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 178491309, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzylimidazole | HCID 77918 | — |
| Product | HCID 178491309 | HCID 178491309 | — |
Reaction Steps
Anisoyl chloride (4.3 ml) was added slowly to a stirred solution of 1-benzylimidazole (5.0 g) in dry acetonitrile (50 ml) keeping the temperature at 25°-30°. After stirring for 1 h. triethylamine (4.4 ml) was added dropwise and the mixture stirred for 18 h. then filtered. The filtrate was concentrated to dryness, and the residue taken up into ether (100 ml) and washed with acetic acid (25%, 3×50 ml), and 2 N sodium carbonate (3×50 ml), then concentrated until the title compound crystallised as a white solid, m.p. 108°-110° (3.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04324792 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-71747a5102304c7da6568401b47aa5ae |
| Source note | uspto-grants-1982_04 |