Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | Sodium Chloride | HCID 5234 | — |
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Edukt | 4-(4-Methoxyphenyl)butyric acid | HCID 78280 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 4-(4-Methoxyphenyl)butanamide | HCID 22566175 | — |
Reaktionsschritte
4-(4-Methoxyphenyl) butyric acid (1) (450 g, 2.32 mole) was combined with dry THF (4 L) and 4-methylmorpholine (268 mL, 2.43 mole) in a 12 L three neck flask with mechanical stirring, an ice-methanol cooling bath and nitrogen atmosphere. Small pieces of dry ice were used to bring the bath temperature below −20° C. Isobutyl chloroformate was added at a rate so as not to exceed an internal temperature of −10° C. After stirring for 30 min. at −10 to −20° C., a 4.7 M solution of ammonia in methanol (990 mL, 4.64 mole) was added in one portion. During the addition, the reaction temperature rose to 0° C. The reaction was allowed to stir for 30 min. and then allowed to stand overnight. The product mixture was transferred to a 22 L separatory funnel with ethyl acetate (6 L), and 10% sodium chloride solution (1.5 L). The layers were separated and the organic solution was washed with 10% sodium chloride solution (4×1 L) and then brine (3×500 mL). The organic layer was dried over sodium sulfate, filtered, evaporated and placed under high vacuum overnight. This afforded 432 g (97%) of the pure amide (117) as an off white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08198286B2 |
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| Quelldatensatz | uspto-grants-2012_06 |
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| ORD ID | ord-d785aa70ceed406db48bb0a054bfb2c2 |
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| Quellennotiz | uspto-grants-2012_06 |
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