Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 2-Pyridyldiphenylphosphine | HCID 621893 | — |
| Katalysator | palladium(II) acetate | HCID 167845 | — |
| Produkt | Methyl propionate | HCID 11124 | — |
| Produkt | Methoxymethyl propionate | HCID 11228781 | — |
Reaktionsschritte
A 250 ml stainless steel, magnetically stirred autoclave was filled with 0.1 mmol palladium(II)acetate, 5 mmol bisphenyl(2-pyridyl)phosphine, 4 mmol p-toluenesulfonic acid, 40 ml (500 mmol) pyridine, 20 ml methanol and 5 g paraformaldehyde. Air was then evacuated from autoclave, and then carbon monoxide (30 bar) and ethene (20 bar) were added. The autoclave was then sealed and heated to a temperature of 110° C. After a reaction time of 5 hours, a sample of the contents of the autoclave was withdrawn and analyzed by gas liquid chromatography. Two products were found; methoxymethylpropionate, which had been formed with a selectivity of 10%, and methylpropionate, which had been formed with a selectivity of 90%. The mean reaction rate was calculated to be 200 mol ethene/gram atom Pd/hour.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05166411 |
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| Quelldatensatz | uspto-grants-1992_11 |
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| ORD ID | ord-60c044af6ebe4e6db57b64cd9b21aca0 |
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| Quellennotiz | uspto-grants-1992_11 |
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