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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979538Generated: October 31, 2026

Benzene → ethyl (E,E)-2-cyano-3,7,11,15-tetramethyl-6,10,14-hexadecatrienoate

https://huagongshe.com/reaction/1979538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantEthyl cyanoacetateHCID 7764—
Reactant5,9,13-Pentadecatrien-2-one, 6,10,14-trimethyl-HCID 61206—
ReactantAmmonium AcetateHCID 517165—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Productethyl (E,E)-2-cyano-3,7,11,15-tetramethyl-6,10,14-hexadecatrienoateHCID 15589936—

Reaction Steps

In 200 ml. of benzene was dissolved 50 g. of farnesyl acetone, and then 28 g. of ethyl cyanoacetate, 5 g. of ammonium acetate and 5 g. of acetic acid were added to the solution. The mixture was then refluxed for 8 hours with removal of the produced water. The reaction mixture then was washed with water and dried. To this mixture there was added dropwise a solution of 4.3 g. of sodium borohydride in 50 ml. of ethanol, under stirring and at 10°-20° C. The stirring was continued for 1 hour. Then, 50 ml. of 10% acetic acid was added to the reaction mixture, and the mixture was subsequently washed with water and dried. The solvent was removed by evaporation and then the residue was purified by silica gel column chromatography to obtain 50.5 g. of the desired oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04481217
Source datasetuspto-grants-1984_11
ORD IDord-871859d79d5b46e2b5e184792751a58e
Source noteuspto-grants-1984_11