참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isopropanol | HCID 3776 | — |
| 반응물 | Trichloroacetic Acid | HCID 6421 | — |
| 반응물 | 2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enal | HCID 3017557 | — |
| 반응물 | Aluminum tri-iso-propoxide | HCID 16685055 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 2-Buten-1-ol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)- | HCID 119897 | 81% |
반응 단계
3.07 g (15 mmol) of Al(O-i-Pr)3 and 30 ml of toluene were fed into a 100 ml four-necked round bottom flask under atmosphere of nitrogen, and stirred at room temperature, and then 28.8 g (150 mmol) of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-al, then 0.25 g (1.5 mmol) of trichloroacetic acid, and further 18.0 g (300 mmol) of isopropyl alcohol were added while stirring at room temperature. Reaction was conducted while fraction containing acetone generated at the solution temperature of 80° to 92° C. was distilled off. After 6 hours, the reaction solution was analyzed by GLC, 81% of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol was obtained (corresponding to 90% selectivity for conversion of the aldehyde as the starting material).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05874649 |
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| 출처 데이터셋 | uspto-grants-1999_02 |
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| ORD ID | ord-3c69ea5d177245898c506b4aba8756cd |
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| 출처 메모 | uspto-grants-1999_02 |
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