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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1385762Erstellt: 27. Oktober 2026

Acetic Acid → 2-Cyclohexene-1,4-diyl Diacetate

https://huagongshe.com/reaction/1385762

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktQuinoneHCID 4650—
Edukt1,3-CyclohexadieneHCID 11605—
EduktLithium acetateHCID 3474584—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelPentaneHCID 8003—
Produkt2-Cyclohexene-1,4-diyl DiacetateHCID 1269643533%

Reaktionsschritte

Lit., J. Org. Chem., 49:4619 (1984). To a stirred solution of 2.8 g (12.5 mmol) palladium acetate, 27.2 g (267 mmol) lithium acetate, and 7.64 g (70.7 mmol) benzoquinone in 200 ml acetic acid at room temperature were added 26.1 g (300 mmol) manganese dioxide and a solution of 23.8 ml (250 mmol) 1,3-cyclohexadiene in 400 ml pentane, and stirring continued for 16 h. The two-phase reaction mixture was separated and the acetic acid phase extracted twice with pentane. The combined organic extracts were washed successively with saturated brine, water, and 2 M sodium hydroxide solution, then the organic phases were dried over sodium sulphate and concentrated in vacuo. Recrystallisation from pentane afforded 16.1 g (33%) of the title compound as an off-white crystalline solid. MS m/e (%): 138 ([M−AcOH]+, 8), 96 ([M−AcOH—COCH2]+, 100), 43 (40).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06262089B1
Quelldatensatzuspto-grants-2001_07
ORD IDord-003a08c81d5743079000eddd05686288
Quellennotizuspto-grants-2001_07