Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 13728613 | HCID 13728613 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13851038 | HCID 13851038 | 41.5% |
Reaction Steps
A mixture of 6-(1-bromo-1-methylethyl)-4-oxo-4H-1-benzopyran-3-carbonitrile (2.0 g), acetic acid (20 ml) and water (5 ml) was heated at 100° C. for one hour, which was then concentrated. The concentrate was subjected to a silica-gel (100 g) column-chromatography, eluting with chloroform-acetone-formic acid (20:1:0.1). The initial eluate was recrystallized from ethanol to give colorless crystals (600 mg) of 6-isopropenyl-4-oxo-4H-1-benzopyran-3-carbonitrile, m.p. 142°-144° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04716167 |
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| Source dataset | uspto-grants-1987_12 |
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| ORD ID | ord-1c90cc9a38c94a28aa37625e0665a17b |
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| Source note | uspto-grants-1987_12 |
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