関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | tert-Butyl hydroperoxide | HCID 6410 | — |
| 反応物 | Ethylbenzene | HCID 7500 | — |
| 反応物 | Tinuvin 770 | HCID 164282 | — |
| 触媒 | Molybdenum oxide | HCID 139765 | — |
| 生成物 | Di-[1-(alpha-methylbenzyloxy)-2,2,6,6-tetramethylpiperidine-4-yl] Sebacate | HCID 19768362 | 70% |
反応手順
A mixture of 40.0 g (83 mmol) of di-(2,2,6,6-tetramethylpiperidin-4-yl) sebacate, 2.0 g of molybdenum oxide, and 250 ml of ethylbenzene is heated to 110° C. (nitrogen atmosphere). A commercially available solution of 70% t-butyl hydroperoxide in water (64.3 g, 499 mmol) is added dropwise over 30 min. Water is collected in a Dean-Stark trap. Heating is continued for 90 minutes after the addition. The reaction mixture is filtered and evaporated. The resulting crude oil is dissolved in heptane (300 ml), and this solution is passed through a short column of silica gel. The first 350 ml of filtrate, nearly pure by TLC, is evaporated to give 41.7 g (70% yield) of the title compound, a viscous oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05204473 |
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| 出典データセット | uspto-grants-1993_04 |
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| ORD ID | ord-4501b9aa0c7c4d44915ad6a18b89cd8e |
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| 出典メモ | uspto-grants-1993_04 |
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