HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 178525959, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-(2-Bromoethyl)naphthalene | HCID 139541 | — |
| Reactant | 4,5-Dichloroimidazole | HCID 140018 | — |
| Reactant | 4-(BROMOMETHYL)PHENOXYACETIC ACID | HCID 7010674 | — |
| Product | HCID 178525959 | HCID 178525959 | — |
Reaction Steps
4,5-dichloroimidazole (1.00 g, 7.36 mmol) was dissolved in acetonitrile. Potassium hydroxide (0.828 g, 14.72 mmol) was added to the solution and allowed to reflux for 30 min. 1 equivalent of 2-(4-(bromomethyl)phenoxy)acetic acid (1.80 g, 7.36 mmol) was added to the solution and refluxed for 5 h. Solution was filtered to remove the KBr precipitate and placed back onto reflux. An equivalent of 2-(2-bromoethylnaphthalene (1.73 g, 7.36 mmol) was added to solution and refluxed for 2.5 h. The solution was neutralized with 6M HBr, volatiles removed in vacuo, and the resulting product will be collected and analyzed.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278951B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-975c6deb09cf457a9fd04412874293d9 |
| Source note | uspto-grants-2016_03 |