Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Veratryl alcohol | HCID 7118 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | Veratryl chloride | HCID 81740 | — |
Reaktionsschritte
3,4-dimethoxybenzyl alcohol (20 g, 119 mmol) was dissolved in toluene (60 ml) and cooled to 0° C. Thionyl chloride (7.48 g, 61.4 mmol) was added dropwise to the cooled solution of the alcohol over a period of 30 minutes, and the reaction was maintained at 0° C. for an additional 30 minutes. The reaction was quenched by pouring onto an ice/water mix (100 ml), and the organic phase was separated. The aqueous phase was then extracted into toluene (2×20 ml) and the combined toluene solution was dried over anhydrous sodium sulfate. The toluene was removed at reduced pressure to afford an oil which solidified upon standing, with a yield of 21 g. The material was characterized as a single spot by thin layer chromatography (TLC).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08895554B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-182dff26fd8a47de90ddcafc14b88847 |
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| Quellennotiz | uspto-grants-2014_11 |
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