Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Decanoic Acid | HCID 2969 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 1-Butoxybut-2-ene | HCID 543904 | — |
| Product | Butanal | HCID 261 | — |
| Product | 1,1-Dibutoxybutane | HCID 22210 | — |
| Product | HCID 347145 | HCID 347145 | — |
Reaction Steps
A glass autoclave was filled with 0.022 g of the catalyst HRuCl(CO)(PPh3)3, 0.031 g of triphenylphosphine, 0.005 g of decanoic acid, 3.18 g (24.8 mmol) of 1-butoxybut-2-ene, 1.83 g (24.8 mmol) of n-butanol and 2.2 g (122 mmol) of water and stirred for 16 hours under autogenous pressure at 155° C. The reaction mixture was analyzed by means of calibrated gas chromatography. At a conversion of 48%, n-butyraldehyde was obtained with a selectivity of 80%, 1-butoxybut-1-ene with a selectivity of 10% and 1,1-dibutoxybutane with a selectivity of 0.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06166265 |
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| Source dataset | uspto-grants-2000_12 |
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| ORD ID | ord-66fb1c0f89e441edaf9740759ff855c3 |
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| Source note | uspto-grants-2000_12 |
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