참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Quinone | HCID 4650 | — |
| 반응물 | 1,3-Cyclohexadiene | HCID 11605 | — |
| 반응물 | Lithium acetate | HCID 3474584 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 촉매 | HCID 178418406 | HCID 178418406 | — |
| 용매 | Pentane | HCID 8003 | — |
| 생성물 | 2-Cyclohexene-1,4-diyl Diacetate | HCID 12696435 | 33% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06262089B1 |
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| 출처 데이터셋 | uspto-grants-2001_07 |
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| ORD ID | ord-003a08c81d5743079000eddd05686288 |
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| 출처 메모 | uspto-grants-2001_07 |
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