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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1-(Benzyloxy)-4-iodobenzeneHCID 519671—
Edukt2-Ethyl-3-methyl-4-trimethylsilanyloxymethyl-cyclohexanoneHCID 18436335—
EduktHCID 178418918HCID 178418918—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-(4-Benzyloxy-phenyl)-2-ethyl-4-hydroxymethyl-3-methyl-cyclohexanolHCID 18436325—

Reaktionsbedingungen

Temperatur25 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07183445B2
Quelldatensatzuspto-grants-2007_02
ORD IDord-c3d8936c17564bbeb3e9057aa27ba592
Quellennotizuspto-grants-2007_02