HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 21329311, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 54270804 | HCID 54270804 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21329311 | HCID 21329311 | — |
Reaction Steps
To a stirred suspension of 4.6 g. (0.016 mole) of the imidazopyridine product of Step C in 175 ml. of acetone, was added 1.8 g. (0.032 mole) of powdered potassium hydroxide. After stirring at room temperature for 20 minutes, 3.9 g. (0.032 mole) of allylbromide was added. Stirring at room temperature was continued overnight and the mixture then was concentrated to one-half volume. The concentrate was diluted with 150 ml. of water and the crude product was collected by filtration. The crude product was crystallized from 70 ml. of ethanol giving 2.0 g. of needles melting at 146°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144341 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-e4699a2cc75d4c08b7f97b5e8bab0889 |
| Source note | uspto-grants-1979_03 |