Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Dipotassium 2,3-dihydroxybutanedioate | HCID 6100505 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | HCID 21891863 | HCID 21891863 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11183440 | HCID 11183440 | 31.7% |
Reaction Steps
A solution of quinolinecarboxylate (obtained in Stage 83f; 1.8 g; 6.7 mmol) in dichloromethane (40 ml) under argon is treated dropwise with diisobutylaluminium hydride (1M in dichloromethane; 20 ml; 20 mmol) at ambient temperature maintained at 10° C. by an ice-cooled water bath. The reaction mixture is agitated for 1 hour at ambient temperature, then poured onto a solution of sodium and potassium tartrate at 20% (200 ml). The resulting mixture is agitated vigorously for 1 hour, then filtered on celite. The filtrate is extracted with dichloromethane (2×100 ml). The combined extracts are washed with water and with a saturated solution of sodium chloride, then dried over magnesium sulphate and concentrated. Purification of the residue by chromatography at medium pressure (SiO2, CH2Cl2/MeOH, 98/2) yields 450 mg of a white solid (m.p.: 176° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135478B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-24218f968e764ae8bb7e488db62a757e |
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| Source note | uspto-grants-2006_11 |
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