HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl bromoacetate → HCID 53926892, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl bromoacetate | HCID 62576 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-[(2,5-Dioxoimidazolidin-4-ylidene)methyl]benzonitrile | HCID 54142030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53926892 | HCID 53926892 | — |
Reaction Steps
6.4 g (0.03 mol) of (5-(4-cyanobenzylidene)-2,4-dioxoimidazolidine and 3.5 g (0.031 mol) of potassium tert-butylate are dissolved in 30 ml of dimethylformamide. After addition of 7.1 g (0.031 mol) of benzyl bromoacetate, the mixture is stirred at room temperature for 7 hours, heated briefly to 100° C. and concentrated. Water is added to the residue, and the mixture is extracted with ethyl acetate. The product crystallises out of the ethyl acetate phase, or can be precipitated by addition of heptane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389614 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-de20046081614173bde1c52f0c7cde91 |
| Source note | uspto-grants-1995_02 |