Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 104093-22-3 | HCID 15760605 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,5-dimethylhexan-1-ol | HCID 262849 | 77.8% |
Reaction Steps
Ethyl 5,5-dimethylhexanoate (1.87 g) (prepared in Example 34 with esterification), was dissolved in 30 ml of THF and lithium aluminium hydride (2 g) added portionwise. The reaction was stirred for 2 hours at 0° C. before quenching with 2 ml 15% NaOH and 6 ml water before diluting with dichloromethane and filtering through CELITE (RTM) and the solvent evaporated to give 5,5-dimethylhexanol product (1.1 g) as a slightly volatile liquid. This alcohol was dissolved in 30 ml dichloromethane containing pyridinium chlorochromate and stirred at room temperature to convert it to the corresponding aldehyde, 5,5-dimethylhexanal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962002 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-ad78d1dda0d14165b206a15060df0477 |
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| Source note | uspto-grants-1999_10 |
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