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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210857Generated: November 1, 2026

Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → 29826-00-4

https://huagongshe.com/reaction/2210857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
Reactant(E)-Dodec-2-en-1-alHCID 5283361—
ReactantEthyl acetate hexaneHCID 21226206—
SolventDichloromethaneHCID 6344—
Product29826-00-4HCID 5312404—

Reaction Steps

To trans-2-dodecenal (4.5 g) dissolved in methylene chloride (80 ml) was added (carbomethoxymethylene)triphenylphosphorane (8.3 g), and the mixture was stirred for 2 hours. The reaction mixture was subjected to chromatography on a silica gel column with eluent systems of n-hexane-ethyl acetate (from 100:1 to 20:1) to give the methyl ester of trans,trans-2,4-tetradecadienoic acid (5.4 g). Potassium hydroxide (6.5 g) was dissolved in a mixed solvent of ethanol-water (1:1) (100 ml). The methyl ester of trans,trans-2,4-tetradecadienoic acid (5.4 g) was added to the mixture, and the resulting mixture was stirred at 60° C. for 40 minutes. After the reaction mixture was cooled, it was adjusted to the weak acidic range of pH with citric acid and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated to give trans,trans-2,4-tetradecadienoic acid (4.4 g). Hereafter, the title compound can be synthesized by the two methods described below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05461036
Source datasetuspto-grants-1995_10
ORD IDord-0a9891fe29b14a84b4c43b2757dac4ef
Source noteuspto-grants-1995_10