HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, 1-isocyanato-4-nitro- → 1-(1-Methyl-2-piperidylidene)-3-(4-nitrophenyl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, 1-isocyanato-4-nitro- | HCID 66012 | — |
| Reactant | 1-Methylpiperidin-2-imine | HCID 12449028 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1-(1-Methyl-2-piperidylidene)-3-(4-nitrophenyl)urea | HCID 54462845 | — |
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 K2CO3 and filtering, a benzene solution of 0.05 mole of p-nitrophenylisocyanate 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-(1-methyl-2-piperidylidene)-3-(4-nitrophenyl)urea:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04046909 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-fe59d770e6b1461699b5cf08b39b8011 |
| Source note | uspto-grants-1977_09 |