Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Bromochlorobenzene | HCID 7806 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 1-Methoxypropa-1,2-diene | HCID 139403 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | N-[4-(1-Hydroxy-2-(1H-imidazol-1-yl)ethyl]phenyl]methanesulfonamide | HCID 13763390 | — |
| Produkt | 1-Chloro-4-(2-propyn-1-yl)benzene | HCID 13660255 | — |
Reaktionsschritte
In a flask containing 59 g (2.43 mole) magnesium turnings in 500 ml anhydrous ether under an atmosphere of nitroge add slowly a solution of 465 g (2.43 mole) of 4-bromochlorobenzene in 1 liter 4 anhydrous ether. With caution, once the Grignard has started maintain slow reflux until all 4-bromochlorobenzene has been added. Stir an additional hour and then add this Grignard (maintain slow reflux) to a suspension of 170 g (2.43 mole) methoxyallene and 69 g of cuprous bromide in 300 ml anhydrous ether under N2. When addition is complete, stir another 10 minutes and then add saturated ammonium chloride. Decant off the ether solution wash the solid residue with ether (3×50 ml). Combine the ether extracts and wash with 1N HCl, saturated aqueous sodium bicarbonate, water and dry over magnesium sulfate. Evaporate off the ether and distill the residue in vacuo to obtain the title compound (99-105mmHg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04613609 |
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| Quelldatensatz | uspto-grants-1986_09 |
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| ORD ID | ord-1d42ee52890f4ac9a7be41fcf2c87f49 |
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| Quellennotiz | uspto-grants-1986_09 |
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