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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258620Generated: October 31, 2026

Acetic Anhydride → HCID 20327652, compound

https://huagongshe.com/reaction/258620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 9885481HCID 9885481—
SolventDiethyl EtherHCID 3283—
ProductHCID 20327652HCID 20327652—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7-[N-4-hydroxynonyl)methanesulfonamido]heptanoic acid (10.9 g., 0.03 mole) (Example 1, Step B) 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 basic solution is separated and acidified with concentrated hydrochloric acid. The crude product 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. There is obtained 7-[N-(4-acetoxynonyl)methanesulfonamido]heptanoic acid as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04033996
Source datasetuspto-grants-1977_07
ORD IDord-2441191741c9426490e88378889d9aed
Source noteuspto-grants-1977_07