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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972818Generated: October 26, 2026

4-Nitrophthalic acid anhydride → 1-Cyclohexyl-4-(4-nitrophthalimido)piperidine

https://huagongshe.com/reaction/972818

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophthalic acid anhydrideHCID 230976—
Reactant1-Cyclohexylpiperidin-4-amineHCID 4778239—
SolventChloroformHCID 6212—
Product1-Cyclohexyl-4-(4-nitrophthalimido)piperidineHCID 21405549—

Reaction Steps

6.85 Grams of 4-amino-1-cyclohexylpiperidine were added to 7.26 grams of 4-nitrophthalic anhydride in 100 milliliters of chloroform and the solution was evaporated to dryness. 50 millilters of acetic anhydride were then added and the solution was heated on a steam bath for half an hour. The excess acetic anhydride was evaporated off and the residue dissolved in 40 millilters of isopropyl alcohol and the product crystallised out. This was filtered, dried and dissolved in the least amount of ethanol and ethereal hydrogen chloride added to give 2.85 grams of the title compound which was collected as the monohydrochloride. Melting Point: 265°-270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04053615
Source datasetuspto-grants-1977_10
ORD IDord-773fa9ea11ee4dd8a10393da312b47f3
Source noteuspto-grants-1977_10