Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (1-Bromoheptyl)benzene | HCID 18417691 | — |
| Reactant | HCID 20524358 | HCID 20524358 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20524460 | HCID 20524460 | — |
Reaction Steps
0.24 g of 55% sodium hydride dispersion in mineral oil were added to a solution of 1.63 g of N-(2,6-dichlorobenzoyl)-N'-(4-hydroxyphenyl)urea in 15 ml of dimethylformamide; the reaction mixture was stirred for 20 minutes with external cooling with water until a bright solution was obtained. 1.6 ml of 77% 1-phenylheptylbromide were added to this solution after which the reaction mixture was left to stand at room temperature for approximately 2 days. After pouring the reaction mixture on a mixture of ice water and petroleum ether a crystalline product was obtained which was sucked off, washed with successively water and little isopropanol and dried in air. The desired product was obtained in a yield of 0.87 g; melting point 146°-149° C. The product was identified by means of its NMR spectrum. The following compounds were prepared in a corresponding manner:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04350706 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-b4948a777f214e429240a2d044565556 |
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| Source note | uspto-grants-1982_09 |
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