HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanide → 3-(m-Chloro-alpha,alpha-dimethylbenzyl)-1-cyclohexyl-1-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanide | HCID 5975 | — |
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | 1-Chloro-3-(2-isocyanatopropan-2-yl)benzene | HCID 21329849 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-(m-Chloro-alpha,alpha-dimethylbenzyl)-1-cyclohexyl-1-methylurea | HCID 21329839 | 90.7% |
Reaction Steps
A solution of 1.2 g of N-methyl-N-cyclohexylamine in 5 ml of n-hexane was added to a solution of 0.01 mole of m-chloro-α,α-dimethylbenzyl isocyanate (prepared from the corresponding cyanide in the same way as shown in Synthesis Example 1) in 10 ml of benzene. The mixture was kept at room temperature for 6 hours and concentrated under reduced pressure to obtain crystals, which were recrystallized from n-hexane to give 2.8 g of the title compound as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04143061 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-38dc2c6bcd744c38b6d1f74a83f09570 |
| Source note | uspto-grants-1979_03 |