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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46953Generated: October 29, 2026

Sodium Acetate → 3,7,11,15,19,23,27,31,35,39,43-Undecamethyl-2,6,10,14,18,22,26,30,34,38,42-tetratetracontaundecaenyl acetate

https://huagongshe.com/reaction/46953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant15575-14-1HCID 5280474—
SolventWaterHCID 962—
SolventAcetic AnhydrideHCID 7918—
Product3,7,11,15,19,23,27,31,35,39,43-Undecamethyl-2,6,10,14,18,22,26,30,34,38,42-tetratetracontaundecaenyl acetateHCID 3053847—

Reaction Conditions

Temperature100 °C

Reaction Steps

3.5 Grams of undecaprenol were dissolved in 15 ml of acetic acid anhydride and the solution was added with 2.0 g of anhydrous sodium acetate at room temperature. The mixture was stirred at 100° C. for one hour to complete the reaction. Upon cooling, the reaction product was poured in water to hydrolyze excessive acetic acid anhydride. After extraction with n-hexane, the extract was washed with water and concentrated. The concentrate was purified by chromatography with 50 g of silica gel in n-hexane/benzene solvent mixture as elution solvent to obtain the final product as white solid (m.p. 36.0°-37.0° C.). Yield 3.5 g.______________________________________Elementary analysis as C57H92O2 : C H______________________________________Theoretical (%): 84.59 11.46Found (%): 84.61 11.46______________________________________

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04175139
Source datasetuspto-grants-1979_11
ORD IDord-1918e4dd231046f4b0ed8ea09c877480
Source noteuspto-grants-1979_11