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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973954Generated: November 4, 2026

4-(Benzyloxy)phenyl isocyanate → 1-(4-Benzyloxyphenyl)-3-(1-methyl-2-piperidylidene)urea

https://huagongshe.com/reaction/1973954

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzyloxy)phenyl isocyanateHCID 256268—
Reactant1-Methylpiperidin-2-imineHCID 12449028—
SolventBenzeneHCID 241—
Product1-(4-Benzyloxyphenyl)-3-(1-methyl-2-piperidylidene)ureaHCID 53915623—

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-benzyloxyphenylisocyanate 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-benzyloxyphenyl)-3 -(1-methyl-2-piperidylidene)urea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998958
Source datasetuspto-grants-1976_12
ORD IDord-1196447e2ba346a48bb709e7db53e587
Source noteuspto-grants-1976_12