Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Water | HCID 962 | — |
| Edukt | 2,3,5,6-Tetrafluorobenzonitrile | HCID 297546 | — |
| Katalysator | Nickel | HCID 935 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 2,3,5,6-Tetrafluorobenzaldehyde | HCID 601331 | — |
Reaktionsschritte
Into a 500 ml-volume glass-made reactor equipped with a condenser tube, 5.00 g of 2,3,5,6-tetrafluorobenzonitrile, 51.00 g of methanol, 52.00 g of water, 45.00 g of acetic acid and 0.50 g of sponge nickel were charged. After purging the vapor phase moiety with hydrogen gas, the mixed solution was stirred at 60° C. under atmospheric pressure while continuously supplying hydrogen. As the time passed, the reaction solution was sampled and analyzed by means of a gas chromatograph. As a result, it was confirmed that 2,3,5,6-tetrafluorobenzyl alcohol was produced together with 2,3,5,6-tetrafluorobenzaldehyde. The yields in the reaction solution are shown in the table below.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06624336B1 |
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| Quelldatensatz | uspto-grants-2003_09 |
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| ORD ID | ord-2843fd65e4114ad7b0200ec157170cfe |
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| Quellennotiz | uspto-grants-2003_09 |
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