Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 2,5-Dihydrofuran | HCID 15570 | — |
| Edukt | 4-Hydroxybutanal | HCID 93093 | — |
| Katalysator | Hastelloy C | HCID 11332432 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Furan | HCID 8029 | — |
| Produkt | 2,3-Dihydrofuran | HCID 70934 | — |
Reaktionsschritte
A 300 ml stirred Hastelloy C autoclave was charged with 16 g 2,5-dihydrofuran, 80 g water and 5 g of the catalyst described in Example III. The autoclave was heated for 3 hours at 120° C. After cooling the resulting liquid was analysed by means of gas-liquid chromatography. The conversion of 2,5-dihydrofuran amounted to 55% gamma-hydroxy butyraldehyde having been formed with a selectivity of 65%. 2,3-Dihydrofuran, tetrahydrofuran and furan had also been formed in minor amounts.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04297517 |
|---|
| Quelldatensatz | uspto-grants-1981_10 |
|---|
| ORD ID | ord-2c2121915bee4d21b2d5558cff8b706c |
|---|
| Quellennotiz | uspto-grants-1981_10 |
|---|
