Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | 2-Dodecylthiophene | HCID 566347 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 5-Dodecylthiophene-2-carbaldehyde | HCID 14985089 | 75,9% |
Reaktionsschritte
In a 1 liter-four-necked flask, 93.7 g (1.28 mol) of N,N-dimethylformamide was placed and cooled to 5° C., followed by addition of 107.4 g (7.00×10-1 mol) of POCl3 in 15 min. below 10° C. under stirring. After stirring for 30 min. below 10° C., 160 g (6.35×10-1 mol) of 2-dodecylthiophene was added dropwise to the mixture in 10 min. at room temperature, followed by stirring for 1.5 hours and further stirring for 2.5 hours at 60° C. After the reaction, the reaction mixture was poured into 2 liter of iced water, subjected to 3 times of extraction with 500 ml of chloroform and washed 6 times with 500 ml of water. The organic layer was dried on CaCl2, followed by distilling-off of the solvent to obtain 237 g of a crude product. The crude product was subjected to reduced-pressure distillation in an atmosphere of nitrogen to obtain 135 g of a product (yield: 75.9%). b.p.: 160° C./0.6 mmHg
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05118441 |
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| Quelldatensatz | uspto-grants-1992_06 |
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| ORD ID | ord-559be8ca61c24572ade9750d3c439cd1 |
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| Quellennotiz | uspto-grants-1992_06 |
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