HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanide → 3-(p-Chloro-alpha,alpha-dimethylbenzyl)-1-ethyl-1-phenylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanide | HCID 5975 | — |
| Reactant | N-Ethylaniline | HCID 7670 | — |
| Reactant | 1-Chloro-4-(2-isocyanatopropan-2-yl)benzene | HCID 13118323 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(p-Chloro-alpha,alpha-dimethylbenzyl)-1-ethyl-1-phenylurea | HCID 21329861 | 98.2% |
Reaction Steps
A solution of 3.9 g of p-chloro-α,α-dimethylbenzyl isocyanate, prepared from the corresponding cyanide in the same way as in Synthesis Example 1, in 20 ml of toluene was added to 2.7 g of N-ethylaniline and the mixture was heated under reflux for 3 hours. After allowing the reaction mixture to cool, the mixture was washed successively with 2N hydrochloric acid, 2N aqueous sodium hydroxide and water. The organic layer was dried over anhydrous sulfate and the solvent was removed by distillation under reduced pressure to obtain 6.2 g of the title compound as a light brown oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04143061 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-3d4c616b4bdf4b13a29d018948a15c8d |
| Source note | uspto-grants-1979_03 |