HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorophenyl Isocyanate → 1-(4-Chlorophenyl)-3-(1-methyl-2-piperidylidene)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorophenyl Isocyanate | HCID 7693 | — |
| Reactant | 1-Methylpiperidin-2-imine | HCID 12449028 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(4-Chlorophenyl)-3-(1-methyl-2-piperidylidene)urea | HCID 53689836 | — |
Reaction Steps
The hydrochloride salt of 2-imino-1-methylpiperidine (7.43 g.; 0.05 mole) is converted to the free base in benzene in the usual manner. After drying over K 2 CO 3 and filtering, a benzene solution of 0.05 mole of p-chlorophenylisocvanate is added dropwise with stirring. After addition is complete, further stirring is continued for about 6 hours at room temperature. The benzene is evaporated in vacuo and the solid residue is recrystallized from methanol to give the product, 1-(4-chlorophenyl)- 3-(1-methyl-2-piperidylidene)urea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998958 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-7dcfc03d3b2641599763f0f53e3db97d |
| Source note | uspto-grants-1976_12 |