Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol | HCID 996 | — |
| Edukt | Diphenyl-3-methyl-3-buten-1-yl phosphate | HCID 131715882 | — |
| Lösungsmittel | Carbon Disulfide | HCID 6348 | — |
| Produkt | 4,4-Dimethylchroman | HCID 316763 | — |
Reaktionsschritte
To a dry, ice-cooled flask containing 34.95 g (0.134 mol) of stannic chloride was added quickly under argon 63.0 g (0.669 mol) of phenol. The mixture was stirred at 0° C. for 0.5 hour and then treated with 43.0 g (0.135 mol) of diphenyl-3-methyl-3-buten-1-yl phosphate, followed by a 5 ml carbon disulfide rinse. The mixture was stirred at room temperature for 21 hours and then quenched by pouring onto 700 g ice and 1 liter of 1.5N NaOH. The mixture was extracted with 1×600 ml and 2×300 ml ether. The combined ether fractions were washed with 2N NaOH, saturated NaCl and dried (MgSO4). Solvent was removed in vacuo and the residue purified by flash chromatography (silica; 2% ether in hexane) to give the title compound as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05089509 |
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| Quelldatensatz | uspto-grants-1992_02 |
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| ORD ID | ord-5da5d3ddcb8d4a4190087f65ba1fc1ba |
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| Quellennotiz | uspto-grants-1992_02 |
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