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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1178388Erstellt: 27. Oktober 2026

Diisopropylethylamine → 4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanone

https://huagongshe.com/reaction/1178388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
Edukt4-(2-Hydroxyethyl)cyclohexan-1-oneHCID 15700392—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-(2-Triisopropylsilanyloxy-ethyl)-cyclohexanoneHCID 21986099—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of 4-(2-hydroxy-ethyl)cyclohexanone (Intermediate R10, 6.8 g, 52.6 mmol, (obtainable as described in the publication by Ciufolini et. al. J. Amer. Chem. Soc. 1991, 113, 8016) was dissolved in CH2Cl2 (75 mL) and treated with diisopropylethylamine (9.2 mL, 52.6 mmol) followed by tri-isopropylsilyl trifluoromethane sulfonate (TIPSTf) (15.3 g, 50.2 mmol) at −30° C. The reaction mixture was warmed to 0° C. for 1 h. The mixture was subjected to an aqueous work-up and purified by chromatography on SiO2 to give 4-(2-triisopropylsilanyloxy-ethyl)-cyclohexanone (Intermediate R11, 11.8 g (82%). Intermediate R11 was converted via Intermediate R12 to the unsaturated aldehyde, 5-(2-triisopropylsilanyloxy-ethyl)-cyclohex-1-enecarbaldehyde (Intermediate R13).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07276522B2
Quelldatensatzuspto-grants-2007_10
ORD IDord-60b9f8f477a34ad38d883259a5ddd9e1
Quellennotizuspto-grants-2007_10