HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium diisopropylamide → 5-(9-Ethoxycarbonylnona-6,8-dienyl)imidazo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Triethyl 4-phosphonocrotonate, mixture of isomers | HCID 5365783 | — |
| Reactant | 5-(5-Formylpentyl)imidazo[1,5-a]pyridine | HCID 23321890 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(9-Ethoxycarbonylnona-6,8-dienyl)imidazo[1,5-a]pyridine | HCID 54055927 | — |
Reaction Steps
To a solution of lithium diisopropylamide (prepared from 3.8 ml of n-butyllithium in hexane and 0.84 ml of diisopropylamine) in 10 ml tetrahydrofuran at -70° C., is added 1.35 g of triethyl 4-phosphonocrotonate in a dropwise manner over a 15 minute period. On completion of the addition, 6.0 g of 5-(5-formylpentyl)imidazo[1,5-a]pyridine is added in a dropwise manner. The reaction mixture is allowed to stir at room temperature for 15 minutes. The reaction mixture is quenched with methanol and the solvent evaporated under reduced pressure to yield 5-(9-ethoxycarbonyl-nona-6,8-dienyl)-imidazo[1,5-a]pyridine as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588732 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-5ff47a749feb4f6cabb6e410800777fd |
| Source note | uspto-grants-1986_05 |