HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 554506Erstellt: 26. Oktober 2026
Water → 1-Benzyloxy-(4-methylsulfanylbenzyl)benzene
https://huagongshe.com/reaction/554506
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylsilane | HCID 12052 | — |
| Edukt | (2-Benzyloxyphenyl)-(4-methylsulfanyl-phenyl)methanol | HCID 67459728 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 1-Benzyloxy-(4-methylsulfanylbenzyl)benzene | HCID 67461294 | 95% |
Reaktionsschritte
In a nitrogen stream, triethylsilane (1.23 mL, 7.72 mmol) and a boron trifluoride-diethyl ether complex (0.88 mL, 5.48 mmol) were added to a solution of (2-benzyloxy-phenyl)-(4-methylsulfanylphenyl)-methanol (2.13 g, 6.3 mmol) in acetonitrile (15 mL) at −40° C. and the mixture solution was stirred at the same temperature for 1.5 hours and further at 0° C. for 30 minutes, and then water was added thereto and the mixture was extracted with methylene chloride. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:10)] to obtain the title compound (1.9 g, 95%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08048897B2 |
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| Quelldatensatz | uspto-grants-2011_11 |
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| ORD ID | ord-496fbf8482264c2abfa287ed2a2af56d |
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| Quellennotiz | uspto-grants-2011_11 |
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