Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Dipropylamine | HCID 8902 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 2-(2-Methyl-3-nitrophenyl)acetic acid | HCID 13530897 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 13530898 | HCID 13530898 | — |
Reaktionsschritte
A mixture of 22.0 g (0.105 mole) of 2-methyl-3-nitrophenylacetic acid and 25 cc of thionyl chloride was slowly heated to 75° and the copious evolution of gasses allowed to moderate. The temperature was raised and the solution was refluxed for 1 hour. The reaction was concentrated in vacuo. The residual straw-colored syrup was chased several times with dry toluene, diluted with 100 cc of dry toluene and added to a cool (10°) mixture of 13 g of sodium carbonate in 150 cc of water and 150 cc of toluene containing 14.5 cc (10.6 g, 0.12 mole) of di-n-propylamine with very slow stirring. After 30 minutes, the ice-bath was removed. Stirring was continued for one hour. An additional 0.5 g of solid sodium carbonate was added to the reaction. After 15 minutes, the organic phase was separated, washed with 5% aqueous sodium carbonate followed by 2N hydrochloric acid and, finally, water. The organic solution was dried over magnesium sulfate, concentrated in vacuo and pumped free of solvent to give 29.5 g of 2-methyl-3-nitrophenyl-N,N-di-n-propylacetamide as a straw-colored syrup.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04588740 |
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| Quelldatensatz | uspto-grants-1986_05 |
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| ORD ID | ord-25f74a1071754ba6ac95766b03eaaa8d |
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| Quellennotiz | uspto-grants-1986_05 |
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