関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | 2-Methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-enal | HCID 3017557 | — |
| 反応物 | Aluminum tri-iso-propoxide | HCID 16685055 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | 2-Buten-1-ol, 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)- | HCID 119897 | 88% |
反応手順
10.2 g (50 mmol) of Al(O-i-Pr)3, 0.25g (2.5 mmol) of sulfuric acid and 180 g (3.0 mol) of IPA were fed into a 1000 ml four-necked round bottom flask under atmosphere of nitrogen, and stirred at 85° C., and then 192 g (1.0 mol) of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-al was added. The reaction was conducted while fraction containing acetone generated at the solution temperature of 85° to 95° C. was removed by distillation. After 7 hours, the reaction solution was analyzed by GLC, 88% of 2-methyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol was obtained (corresponding to 92% selectivity for conversion of the aldehyde as the starting material).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05874649 |
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| 出典データセット | uspto-grants-1999_02 |
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| ORD ID | ord-a8b69d3c19ed4602a7ee490ddb24ac2a |
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| 出典メモ | uspto-grants-1999_02 |
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