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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081312Generated: November 1, 2026

Iodine → 4-[2-[(E)-2-iodovinyl]-phenoxy]butyric acid ethyl ester

https://huagongshe.com/reaction/2081312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactanttrans-1,2-Bis(tri-n-butylstannyl)ethyleneHCID 5378370—
Reactant4-(2-Iodophenoxy)butyric acid ethyl esterHCID 15070115—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
Product4-[2-[(E)-2-iodovinyl]-phenoxy]butyric acid ethyl esterHCID 15070120—

Reaction Steps

1.34 g of (4-(2-iodophenoxy)-butyric acid ethyl ester and 6.4 g of (E)-1,2-bis-(tri-n-butylstannyl)-ethylene (50%) are dissolved in 12 ml of toluene, mixed with 94 mg of tetrakis-(triphenylphosphine)-palladium and heated with stirring and argon atmosphere for 2 hours to 70°-80° C. (bath temperature). After cooling to room temperature, the reaction mixture is diluted with 12 ml of diethyl ether and treated with a solution of 2.04 g of iodine in 10 ml of diethyl ether, worked up and chromatographed on silica gel with n-hexane/ethyl acetate=95/5 under the conditions of example 2C. 900 mg of 4-[-[(E)-2-iodovinyl]-phenoxy]-butyric acid ethyl ester is obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183925
Source datasetuspto-grants-1993_02
ORD IDord-249d52b406a34fccbb90544f0eb470a8
Source noteuspto-grants-1993_02