HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 991281Erstellt: 27. Oktober 2026
p-(Trifluoromethoxy)benzaldehyde → 4-(Trifluoromethoxy)benzenemethanol
https://huagongshe.com/reaction/991281
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | p-(Trifluoromethoxy)benzaldehyde | HCID 69573 | — |
| Edukt | Sodium Formate | HCID 2723810 | — |
| Katalysator | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(Trifluoromethoxy)benzenemethanol | HCID 137184 | — |
Reaktionsschritte
8.55 g of 4-trifluoromethoxybenzaldehyde, 0.63 g of bis(triphenylphosphine) palladium dichloride and 6.12 g of sodium formate were placed in a flask fitted with a reflux condenser, 45 ml of DMF were added and the mixture was stirred and heated at 110° C. The course of the reaction was monitored by means of GC. After conversion was complete (GC monitoring), the reaction mixture was allowed to cool to 21° C. and the catalyst was separated off by filtration through silica gel. The filter was rinsed with methyl tert-butyl ether and the filtrate washed with 3×100 ml of water in order to remove the DMF. This gave 6.0 g (69% of theory) of 4-trifluoromethoxybenzyl alcohol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06462242B1 |
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| Quelldatensatz | uspto-grants-2002_10 |
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| ORD ID | ord-b679be3d4e484e96b9d1d463d6c43255 |
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| Quellennotiz | uspto-grants-2002_10 |
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