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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071525Generated: November 1, 2026

Benzene, 1-isocyanato-4-nitro- → 1-(1-Methyl-2-piperidylidene)-3-(4-nitrophenyl)urea

https://huagongshe.com/reaction/2071525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-isocyanato-4-nitro-HCID 66012—
Reactant1-Methylpiperidin-2-imineHCID 12449028—
SolventBenzeneHCID 241—
Product1-(1-Methyl-2-piperidylidene)-3-(4-nitrophenyl)ureaHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04046909
Source datasetuspto-grants-1977_09
ORD IDord-fe59d770e6b1461699b5cf08b39b8011
Source noteuspto-grants-1977_09