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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 420238Erstellt: 26. Oktober 2026

Hydrochloric Acid → Ethyl 2-(1-hydroxycyclohex-2-en-1-yl)acetate

https://huagongshe.com/reaction/420238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
Edukt2-Cyclohexen-1-oneHCID 13594—
EduktHCID 178472539HCID 178472539—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 2-(1-hydroxycyclohex-2-en-1-yl)acetateHCID 56644387%

Reaktionsschritte

Under nitrogen atmosphere, 20 mL of ethyl acetate was added to 3.05 g (5 mmol, 1.0 equivalent) of (BrZnCH2COOEt.THF)2. Under argon atmosphere, a solution of 0.48 g (5 mmol) of 2-cyclohexen-1-one in 5 mL of ethyl acetate was added dropwise while stirring at 0˜5° C. The mixture was stirred at 0˜5° C. for 3 hours. 10 mL of 1N hydrochloric acid was added dropwise at 20° C. or lower, followed by dilution with 25 mL of ethyl acetate. Then, the layers were separated. The organic layer was washed successively with 5 mL (×2) of 1N hydrochloric acid, 5 mL (×2) of an aqueous saturated sodium chloride solution, 10 mL (×2) of an aqueous saturated sodium bicarbonate solution, and 10 mL of an aqueous saturated sodium chloride solution. After washing, the organic layer was dried with anhydrous magnesium sulfate. Concentration under reduced pressure afforded 0.80 g of the desired product (yield 87%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093403B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-f231fe79055847a1b26a3b7c452af06a
Quellennotizuspto-grants-2012_01