HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351439Erstellt: 24. Oktober 2026
Hydrochloric Acid → 1-(4-Benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanol
https://huagongshe.com/de/reaction/351439
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 1-(Benzyloxy)-4-iodobenzene | HCID 519671 | — |
| Edukt | 2-Ethyl-3-methyl-4-trimethylsilanyloxymethyl-cyclohexanone | HCID 18436335 | — |
| Edukt | HCID 178418918 | HCID 178418918 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 1-(4-Benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanol | HCID 18436325 | — |
Reaktionsschritte
1-Benzyloxy4-iodo-benzene (5.70 g, 18.37 mmol) was dissolved in anhydrous THF (36 mL) at −10° C. Isopropyl magnesium chloride (1.0 M, 18.37 mL) was added and the mixture was stirred for 3 h. A solution of 2-ethyl-3-methyl-4-trimethylsilanyloxymethyl-cyclohexanone (12.0 g in 50 mL THF) was added slowly over 30 min by syringe pump. The reaction mixture was stirred for 30 min at 25° C. and then refluxed for 30 min. The reaction mixture was then cooled to 25° C., HCl (1.0 N, 80 mL) was added slowly, followed by addition of ethyl acetate (100 mL). The organic layer was washed with H2O (100 mL), dried over MgSO4 and purified on SiO2 (10˜15% ethyl acetate/hexane) to yield 1-(4-benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07183445B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-c3d8936c17564bbeb3e9057aa27ba592 |
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| Quellennotiz | uspto-grants-2007_02 |
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