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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729931Generated: October 25, 2026

Acetic Anhydride → 7-{[4-(Acetyloxy)nonyl](carbamoyl)amino}heptanoic acid

https://huagongshe.com/reaction/1729931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant7-[Carbamoyl(4-hydroxynonyl)amino]heptanoic acidHCID 21501441—
SolventDiethyl EtherHCID 3283—
Product7-{[4-(Acetyloxy)nonyl](carbamoyl)amino}heptanoic acidHCID 53945703—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7-[1-(4hydroxynonyl)ureido]heptanoic acid (9.9 g., 0.03 mole) (Example 1, Step C) and acetic anhydride (6.1 g., 0.06 mole) is heated at 60° C. for 18 hours. The mixture is cooled and taken up in 80 ml. of ethyl ether. The solution is extracted with an ice-cold solution of 8 g. of sodium hydroxide in 150 ml. of water. The basis solution is separated and acidified with concentrated hydrochloric acid. The oil that separates is extracted into ether, washed with water and dried over sodium sulfate. The ether is evaporated and the residual oil is purified by chromatography on silica gel using 2% methanol in chloroform as the eluting solvent. Thus there is obtained 7-[1-(4-acetoxynonyl)ureido] heptanoic acid as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989749
Source datasetuspto-grants-1976_11
ORD IDord-537c0d46c6654f0a888984f8e49d2622
Source noteuspto-grants-1976_11