Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Quinoline, 1,2-dihydro-1-acetyl- | HCID 82423 | 44% |
Reaction Steps
Quinoline (19.37 g, 150 mmol) was dissolved in anhydrous diethyl ether (500 ml) and cooled to 0° C. under inert atmosphere. DIBAL, 1.5 M in toluene (100 ml, 150 mmol) was added dropwise over 2 hrs and the reaction mixture was stirred at 0° C. for 30 min. Acetic anhydride (500 ml) was added dropwise over 30 min and the reaction mixture was stirred at 0° C. for 30 min. H2O was added cautiously. The reaction mixture was extracted with diethyl ether and concentrated to give N-acetyl-1,2-dihydroquinoline (11.5 g, 44%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517992B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-5373c13aa88d408fa314936f77500c39 |
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| Source note | uspto-grants-2009_04 |
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