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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275477Generated: October 30, 2026

Maleic Anhydride → HCID 86748487, compound

https://huagongshe.com/reaction/275477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMaleic AnhydrideHCID 7923—
Reactant13-Docosen-1-amine, (13Z)-HCID 20841368—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 86748487HCID 8674848796.2%

Reaction Conditions

Temperature75 °C

Reaction Steps

A 250 ml, 3-neck flask equipped with a stirrer, thermometer, Dean-Stark receiver and condenser was charged with 18 g of maleic anhydride (0.18 mole) and 60 ml carbon tetrachloride. Erucyl amine (59.0 g, 0.18 mole) was added dropwise at 70° C. under a nitrogen atmosphere. The mixture was stirred at 75° C. for 4 hours. The temperature was raised to 90° C. to distill out carbon tetrachloride and the mixture was then stripped at 100° C. 10 mmHg vacuum for 15 minutes to afford 73 g of N-Erucyl-maleic acid monoamide. An IR spectrum indicated the presence of amide and carboxyl groups. This product had an acid number of 135; no total amine value; a saponification value of 137.6; a melting point of 55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05393814
Source datasetuspto-grants-1995_02
ORD IDord-e0ef28c12dca4c2382821b432ae8b3c6
Source noteuspto-grants-1995_02