HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1765973Erstellt: 25. Oktober 2026
Propofol → 2-(Chloromethoxy)-1,3-diisopropylbenzene
https://huagongshe.com/reaction/1765973
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Propofol | HCID 4943 | — |
| Edukt | Bromochloromethane | HCID 6333 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Produkt | 2-(Chloromethoxy)-1,3-diisopropylbenzene | HCID 11253147 | — |
Reaktionsschritte
2,6-Diisopropylphenol (20 kg, FW (formula weight)=178, 112 mol, 1 equiv.) is reacted with bromochloromethane (347 kg, FW=129, 2,682 mol, 24 equiv.) and sodium hydroxide (11 kg, FW=40, 280 mol, 2.5 equiv.) in tetrahydrofuran (108 kg, FW=72, 1,498 mol, 13.3 equiv.) at reflux for approximately 1.5 hours. After cooling to 20° C., the reaction mixture is quenched with water (87 kg). The organic layer is collected and washed with 15% sodium chloride aqueous solution (78 kg) twice. The organic layer is collected again after the layer separation, and the solvents are distilled from the organic layer to afford a crude oil. The crude oil is distilled by simple distillation to yield a purified chloromethyl(2,6-diisopropylphenyl)ether (FW=227) as a light yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07229978B2 |
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| Quelldatensatz | uspto-grants-2007_06 |
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| ORD ID | ord-1600d33c30254157ac0fe74bb7c7698c |
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| Quellennotiz | uspto-grants-2007_06 |
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