HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 21329312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 21329329 | HCID 21329329 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 21329312 | HCID 21329312 | — |
Reaction Steps
Treat a suspension of 1.4 g. (0.005 mole) of the imidazopyridine product of Step D in 80 ml. of acetone with 560 mg. (0.01 mole) of powdered potassium hydroxide. Stir at room temperature for 20 minutes and add 1.21 g. (0.01 mole) of allyl bromide. Continue stirring overnight. Concentrate the reaction mixture to one-half volume and dilute with 75 ml. of water. Separate the solid product by filtration and crystalize from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144341 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-46273e5a4c5446e7a204e024daa10ae4 |
| Source note | uspto-grants-1979_03 |