Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propanal | HCID 527 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,5,5-Trimethylhexanal | HCID 21574 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3,5,5-Trimethylhexanal | HCID 21574 | — |
| Product | 2,5,7,7-Tetramethyloct-2-enal | HCID 53997384 | — |
Reaction Steps
128 g (4 moles) of methanol and 2 g (0.05 mole) of NaOH were initially taken under nitrogen in a reaction flask and were refluxed. A mixture of 142 g (1 mole) of 3,5,5-trimethylhexanal and 116 g (2 moles) of propionaldehyde was added dropwise to this solution in the course of 10 minutes. The resulting reaction mixture was kept at the boil for 1 hour (h) and then brought to pH 4-5 with an 80% strength aqueous acetic acid solution. After washing twice with water, the organic phase was separated off and worked up by fractional distillation. 32 g of unconverted 3,5,5-trimethylhexanal, as light ends, and 113 g of 2,5,7,7-tetramethyl-2-octenal (bp.=108°-111° C./14 mbar) were obtained, corresponding to a selectivity of 81%, based on trimethylhexanal; nD25 =1.4580.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04758548 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-2e74adac17c54f08951ed687b778ed36 |
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| Source note | uspto-grants-1988_07 |
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