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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 271835Erstellt: 25. Oktober 2026

Cyclohexanone → HCID 59836431, Verbindung

https://huagongshe.com/reaction/271835

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCyclohexanoneHCID 7967—
EduktAcetic acid, 2,2-dimethoxy-, methyl esterHCID 66647—
EduktLithium HexamethyldisilazideHCID 2733832—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 59836431HCID 59836431—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

Cyclohexanone Compound 2a (1.37 g, 14.0 mMol) in THF (5 mL) was added dropwise to a solution of LHMDS (16.0 mL, 16.0 mMol) in anhydrous THF (25 mL) at −78° C. under a N2 atmosphere. The solution was stirred at −78° C. for about 1 hr. Methyl dimethoxyacetate Compound 11a (1.88 g, 14.0 mMol) in anhydrous THF (5 mL) was then added dropwise. The reaction mixture was stirred while warming to r.t. over a period of about 15 hrs, then the reaction was quenched with water (5 mL). The organic layer was diluted with EtOAc (100 mL) and washed with water and brine. The organic layer was separated and dried with anhydrous sodium sulfate, then filtered and concentrated in vacuo to yield a crude product as an oil. The oil was purified by flash chromatography (eluted with 10% EtOAc in hexane) to afford 2-(2,2-dimethoxy-acetyl)-cyclohexanone Compound 11b (1.82 g, 65%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07452997B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-82e679f6918c48e7a2ce22440d538ded
Quellennotizuspto-grants-2008_11