HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 86749626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(diphenylmethyleneamino)acetate | HCID 319508 | — |
| Reactant | 4-(Benzoxazol-2-yl)benzyl bromide | HCID 11033515 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86749626 | HCID 86749626 | — |
Reaction Steps
A mixture of N-(diphenylmethylene)glycine ethyl ester (6.85 g; 25.6 mmol), 4-(benzoxazol-2-yl)benzyl bromide (7.37 g; 25.6 mmol), tetrabutylammonium bromide (0.83 g; 2.6 mmol); potassium carbonate (10.6 g; 77 mmol) and dry acetonitrile (50 ml) is heated at reflux 4 hours. The reaction is cooled and diluted with CH2Cl2, washed with water, dried (Na2SO4) and concentrated in vacuo to yield ethyl 2-[4-(benzoxazol-2-yl)benzyl]-N-(diphenylmethylene)-glycine as an oil which is used directly without further purification in Step B.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534532 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-6e2bbebe16d74a66884e007d1839f371 |
| Source note | uspto-grants-1996_07 |