Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397628Generated: October 29, 2026

Acetic Anhydride → HCID 21436333, compound

https://huagongshe.com/reaction/2397628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 21436323HCID 21436323—
SolventEthyl AcetateHCID 8857—
ProductHCID 21436333HCID 21436333—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 7-[3-(3-hydroxyoctyl)-4-oxo-2-thiazolidinyl]heptanoic acid (9.0 g., 0.025 mole) and acetic anhydride (0.1 g., 0.06 mole) is heated at 60° C. for 18 hours. The resulting mixture is cooled to room temperature and dissolved in ethyl acetate providing a clear solution which is extracted with an ice-cold solution of sodium hydroxide (8 g.) in water (150 ml.). The basic solution is quickly separated and acidified with concentrated hydrochloric acid. The oily acid which separates is extracted with ether. The organic extract is washed with water, dried over sodium sulfate, and filtered. Evaporation of the filtrate in vacuo at 40° to 50° C. leaves a residual oil which is purified via application to a silica gel (150 g.) column with chloroform. Elution with chloroform-methanol (99.1; v:v) provides the title compound as a colorless, viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022794
Source datasetuspto-grants-1977_05
ORD IDord-9bddfaf9a2144b3186200b985d1f9466
Source noteuspto-grants-1977_05