HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 12915849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one | HCID 88638 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12915849 | HCID 12915849 | 82.2% |
Reaction Steps
To a solution comprising 2.3 g of 4-(2-keto-1-benzimidazolinyl)-piperidine, 1.1 g of triethylamine, and 20 ml of chloroform is added 2.2 g of phenacyl bromide, and the reaction is carried out under the same conditions as in Example 1. The same post-treatment as in Example 1 is conducted to obtain 3.2 g of a crude product. Recrystallization of the product from a mixture solution of ethanol and ethyl acetate (2:3 by volume) yields 2.92 g of 1-[2-oxo-2-phenyl-1-ethyl]-4-(2-keto-1-benzimidazolinyl)-piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04446141 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-26f8c48a98e3425982439f9ec31b432b |
| Source note | uspto-grants-1984_05 |