Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | 4-((3,4,5-Trimethoxybenzyl)thio)phenol | HCID 384136 | — |
| Katalysator | chromium (VI) trioxide | HCID 10219390 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-((3,4,5-Trimethoxybenzyl)sulfinyl)phenol | HCID 384137 | 66% |
Reaktionsschritte
3,4,5-Trimethoxybenzyl 4-hydroxyphenyl thioether (500 mg, 1.63 mmol), prepared as described in Example 1, was dissolved in 10 mlof acetic acid, and heated to 80° C. A solution of chromium trioxide in 30 ml of distilled water was added dropwise to the above solution. The mixture was stirred for 30 min, cooled to room temperature, diluted with 20 ml of water, and then extracted with 30 ml of ethyl acetate. The organic layer was dried over magnesium sulfate, concentrated and purified on silica gel column chromatography (ethyl acetate/n-hexane=1/4) to give 348 mg (66% yield) of 3,4,5-trimethoxybenzyl 4-hydroxyphenyl sulfoxide as a white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05840991 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-e92c83b6fc5c41b6952ad2903c7a142b |
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| Quellennotiz | uspto-grants-1998_11 |
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