Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 18509495 | HCID 18509495 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 18509424 | HCID 18509424 | 57.4% |
Reaction Steps
Compound 78 (2.00 g; 5.78 mmol) was dissolved in tetrahydrofran (20 ml). While the solution was stirred at −30° C. under nitrogen atmosphere, n-butyl lithium in n-hexane (1.56 M: 3.70 ml; 5.77 mmol) was added dropwise, followed by stirring for 5 minutes. The mixture was cooled to −75° C., and propionaldehyde (1 ml) was slowly added dropwise thereto. The resultant mixture was brought to room temperature over 2 hours, and the reaction was stopped by dropwise addition of saturated aqueous ammonium chloride solution, followed by extraction with diethyl ether (100 ml). The organic layer was washed with saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=5:1), to thereby yield 1.08 g of the target compound as yellow oily matter (yield: 57.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586633B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-1ff0efe6dd604172a47285a9adfb12ba |
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| Source note | uspto-grants-2003_07 |
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