Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21568950 | HCID 21568950 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21568956 | HCID 21568956 | — |
Reaction Steps
A solution of 4,5-dimethyl-6-oxo-7-isopropyl1,2,7,8-tetrahydro-6H-indeno[5,4-b]furan-2-carboxylic acid (0.01 mole) in dimethylformamide (50 ml.) at 15°C. is treated with sodium hydride (50% dispersion in mineral oil, (0.-25 mole). The solution is warmed to 50°C., cooled to 25°C., treated with methyl iodide (0.025 mole) then warmed to 50°C. Thereafter, water (50 ml.) and 10 N sodium hydroxide (2 ml.) are added; the reaction is heated at 95°C. for 0.5 hours then poured into cold 1.0N hydrochloric acid to afford 4,5,7-trimethyl-6-oxo-7-isopropyl-1,2,7,8-tetrahydro-6H-indeno[5,4-b]furan-2-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03931239 |
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| Source dataset | uspto-grants-1976_01 |
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| ORD ID | ord-b832a26e8c7041b49bd13754c7d168e2 |
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| Source note | uspto-grants-1976_01 |
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