Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 20524446 | HCID 20524446 | — |
| Reactant | HCID 178514229 | HCID 178514229 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20524441 | HCID 20524441 | — |
Reaction Steps
1.0 g of 50% sodium hydride dispersion in mineral oil was added at room temperature to a solution of 4.0 g of 2-bromobenzoyl amide in 25 ml of dry acetonitrile. After stirring for approximately 30 minutes at room temperature, 4.78 g of 4-(1-phenylethoxy)phenylisocyanate were added, the reaction mixture becoming warm and substantially homogeneous. After stirring for another approximately 16 hours at room temperature the reaction mixture was filtered. The filtrate was acidified with dilute hydrochloric acid. The resulting precipitate was sucked off and washed successively with acetonitrile, ethanol and petroleum ether (40-60). The desired product was obtained in a yield of 1.85 g; the melting point was determined on a "Kofler bank" and was 155.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04350706 |
|---|
| Source dataset | uspto-grants-1982_09 |
|---|
| ORD ID | ord-29057b0030734d63b126458aae0b1065 |
|---|
| Source note | uspto-grants-1982_09 |
|---|