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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | {[2-(2-Acetoxyethyl)-6,7-dichloro-2,3-dihydro-1-oxo-1H-inden-5-yl]oxy}acetonitrile | HCID 20148936 | — |
| Reactant | Diazabicyclo[4.3.0]non-5-ene | HCID 21585024 | — |
| Catalyst | Diazabicyclo[4.3.0]non-5-ene | HCID 21585024 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {[2-(2-Acetoxyethyl)-6,7-dichloro-2,3-dihydro-1-oxo-2-(3-oxobutyl)-1H-inden-5-yl]oxy}acetonitrile | HCID 20148940 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731471 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-a44c4640c76245ea9b3702fd97263d87 |
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| Source note | uspto-grants-1988_03 |
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