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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569304Generated: October 30, 2026

Methyl vinyl ketone → {[2-(2-Acetoxyethyl)-6,7-dichloro-2,3-dihydro-1-oxo-2-(3-oxobutyl)-1H-inden-5-yl]oxy}acetonitrile

https://huagongshe.com/reaction/569304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl vinyl ketoneHCID 6570—
ReactantEthyl AcetateHCID 8857—
Reactant{[2-(2-Acetoxyethyl)-6,7-dichloro-2,3-dihydro-1-oxo-1H-inden-5-yl]oxy}acetonitrileHCID 20148936—
ReactantDiazabicyclo[4.3.0]non-5-eneHCID 21585024—
CatalystDiazabicyclo[4.3.0]non-5-eneHCID 21585024—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
Product{[2-(2-Acetoxyethyl)-6,7-dichloro-2,3-dihydro-1-oxo-2-(3-oxobutyl)-1H-inden-5-yl]oxy}acetonitrileHCID 20148940—

Reaction Conditions

Temperature40 °C

Reaction Steps

{[2-(2-Acetoxyethyl)-6,7-dichloro-2,3-dihydro-1-oxo-1H-inden-5-yl]oxy}acetonitrile (3.42 g, 10 mMole) is dissolved in tetrahydrofuran (30 ml), warmed to 40° C. and diazabicyclo[4.3.0]non-5-ene (50 microliters) added. Then methyl vinyl ketone (1.2 g, 17 mMole) is added and the mixture stirred at 50°-52° C. for two hours. More methyl vinyl ketone (600 mg) and diazabicyclo[4.3.0]non-5-ene (2 drops) are added and stirring and heating continued for another 2 hours. The solution is cooled, treated with ethyl acetate (50 ml) and poured into ice water (250 ml) containing acetic acid (1 ml). The organic layer is separated and the aqueous layer extracted first with methylene chloride and then with ether. The combined organic layers were dried over MgSO4 and the solvent removed by evaporation in vacuo to give the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731471
Source datasetuspto-grants-1988_03
ORD IDord-a44c4640c76245ea9b3702fd97263d87
Source noteuspto-grants-1988_03