Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 2-Bromo-4-isopropylaniline | HCID 521337 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-Bromo-3-isopropylbenzene | HCID 138499 | — |
Reaktionsschritte
To a mixture of 1000 ml of 96% ethanol and 94 ml of 98% H2SO4, 117 g (0.55 mol) of 2-bromo-4-isopropylaniline was added over 15 min. with vigorous stirring at −5° C. Then, a solution of 63 g of NaNO2 in 125 ml of water was added at this temperature over 1 h, and the resulting mixture was stirred for about 30 min longer. Then, 12 g of copper powder was added. The reaction mixture was refluxed for 4 h and filtered through a glass frit (G3). The filtrate was poured into 2500 cm3 of cold water. The organic product was extracted with 4×400 ml of dichloromethane. The combined extract was dried over K2CO3 and evaporated to dryness. Fractional distillation gave the title product, b.p. 64-67° C./3 mm Hg. Yield 117.4 g (75%) of yellowish oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07910783B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-8564bf82ead246119b8223ba75d0a8ae |
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| Quellennotiz | uspto-grants-2011_03 |
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