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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372534Generated: October 30, 2026

Acetic Anhydride → HCID 20327652, compound

https://huagongshe.com/reaction/372534

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 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 numberUS04091107
Source datasetuspto-grants-1978_05
ORD IDord-87a23dd6e5744a24aa8abb12b3ffec74
Source noteuspto-grants-1978_05