HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 53998100, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1-(1-Benzyl-1H-imidazol-5-yl)ethan-1-one | HCID 11615368 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53998100 | HCID 53998100 | — |
Reaction Steps
1.0 g of magnesium turnings are covered with 5 ml of dry tetrahydrofuran. To the mixture is added 7.8 g of (2-bromoethyl)benzene in 30 ml of dry tetrahydrofuran at such a rate that a smooth reaction is maintained. The mixture is then heated under reflux for one hour. After being cooled to room temperature, 3.0 g of 1-(3-benzyl-3H-imidazol-4-yl)-ethanone in 20 ml of tetrahyrofuran is added dropwise to the Grignard reagent and the reaction mixture is refluxed for one hour. The cooled reaction mixture is poured into a cold dilute hydrochloric acid solution. Work-up of the mixture gives the crude product, which is recrystallized from ethyl acetate. The yield is 3.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06479530B2 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-bb3ae9594bcf423095d9870f8c18eaff |
| Source note | uspto-grants-2002_11 |