Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tert-Butylamine | HCID 6385 | — |
| Edukt | o-Benzylbenzoic acid | HCID 11924 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | N-tert.butyl-alpha-phenyl-o-toluamide | HCID 20385869 | — |
Reaktionsschritte
To a mixture of 49.8 g. (0.235 mole) α-phenyl-o-toluic acid, 300 ml. ether and 10 ml. pyridine, add dropwise with stirring 25 ml. (0.35 mole) of thionyl chloride. The resulting mixture is stirred 21 hours at room temperature then filtered and the solvent removed in vacuo. The resulting acid chloride is dissolved in 150 ml. ether and added dropwise to 35.7 g (0.48 mole) of tert.butylamine in 500 ml. of ethyl ether, and the mixture cooled to 0° C. After addition is complete the resulting mixture is stirred 1 hour at room temperature, the layers separated, the ether washed with 100 ml. of water, 100 ml. of 2 N sodium hydroxide and then with water again, dried over magnesium sulfate, filtered and evaporated to give N-tert.butyl-α-phenyl-o-toluamide; m.p. 91°-92° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04175191 |
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| Quelldatensatz | uspto-grants-1979_11 |
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| ORD ID | ord-79756d4797e94dc0b2b90da49ea04e91 |
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| Quellennotiz | uspto-grants-1979_11 |
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