HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1672380Erstellt: 25. Oktober 2026
Imidazole → (1-(((tert-Butyldimethylsilyl)oxy)methyl)cyclopropyl)methanol
https://huagongshe.com/reaction/1672380
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Imidazole | HCID 795 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Edukt | 1,1-Bis(hydroxymethyl)cyclopropane | HCID 4101437 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (1-(((tert-Butyldimethylsilyl)oxy)methyl)cyclopropyl)methanol | HCID 59000904 | — |
Reaktionsschritte
1,1-Bis(hydroxymethyl)cyclopropane (1.0 g, 0.0098 mol), triethylamine (TEA) (2.0 mL, 0.015 mol), and 1H-imidazole (0.13 g, 0.0020 mol) were dissolved in anhydrous DCM (15 mL) and the solution was cooled to 0° C. A solution of tert-butyldimethylsilyl chloride (1.55 g, 0.0103 mol) in DCM (5 mL) was added drop-wise and the resulting mixture was allowed to warm to RT and stirred overnight. The reaction was quenched with saturated aqueous NaHCO3 and extracted with DCM (3×). The organic extract was dried (magnesium sulfate), filtered, and concentrated in vacuo. The crude product was identified by 1H NMR and used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07998959B2 |
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| Quelldatensatz | uspto-grants-2011_08 |
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| ORD ID | ord-6d2e0e14f7764fbca3d2d7096d880b54 |
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| Quellennotiz | uspto-grants-2011_08 |
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