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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1385762생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1385762

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물QuinoneHCID 4650—
반응물1,3-CyclohexadieneHCID 11605—
반응물Lithium acetateHCID 3474584—
촉매palladium(II) acetateHCID 167845—
촉매HCID 178418406HCID 178418406—
용매PentaneHCID 8003—
생성물2-Cyclohexene-1,4-diyl DiacetateHCID 1269643533%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06262089B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-003a08c81d5743079000eddd05686288
출처 메모uspto-grants-2001_07