Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Dimethyl malonate | HCID 7943 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Iodothiophene | HCID 66332 | — |
| Katalysator | copper(I) bromide | HCID 24593 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Quinoline | HCID 7047 | — |
| Produkt | Dimethyl 3-thienylmalonate | HCID 12509453 | — |
Reaktionsschritte
In the way described before 5.3 g (=0.040 mole) dimethyl malonate were mono-deprotonated with 0.040 mole NaH in 75 ml quinoline. Then 6.7 g (=0.032 mole) 3-iodothiophene and 4.6 g (=0.032 mole) copper (I) bromide were added. The resulting mixture was stirred under N2 atmosphere during a period of 4.5 hours at a temperature of 80° C. and then poured out into a mixture of 75 ml water and 75 ml concentrated HCl. The precipitated copper salts were collected on a Buchner funnel and washed with chloroform. Extraction of the filtrate occured likewise with chloroform. Both chloroform layers were joined and dried over magnesium sulphate. After removal of the solvent 11.0 g of an oily product remained in which by GLC analysis the presence was demonstrated of 1.93 g 3-iodothiophene and 1.32 g di-methyl 3-thienylmalonate (=0.006 mole or 19% calculated to the 3-iodothiophene started from). The product was identified in the same way as described in Example 5.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04262129 |
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| Quelldatensatz | uspto-grants-1981_04 |
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| ORD ID | ord-2bddfd2d3a2d4d7e9c8642a7b0b6c7b8 |
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| Quellennotiz | uspto-grants-1981_04 |
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