関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,3-Cyclohexanedicarboxylic acid | HCID 107205 | — |
| 溶媒 | Acetic Anhydride | HCID 7918 | — |
| 生成物 | 3-Oxabicyclo[3.3.1]nonane-2,4-dione | HCID 419506 | 86% |
反応手順
A suspension of 1,3-cyclohexanedicarboxylic acid (490 g, 2.88 mol) in acetic anhydride (1500 ml) was heated to 140° C., refluxing for 2 hours. Acetic anhydride was then removed with distillation (oil bath 180° C). To the residue was added acetic anhydride (1000 ml) and refluxed at 140° C. for 1 hour. The acetic anhydride was removed again with distillation (under house vacuum, about 50° C.). After crystals appeared, the mixture was cooled to room temperature and MTBE (400 ml) was added. The mixture was then cooled to 0-5° C. The crystals were filtered, washed with MTBE (250 ml), and dried under house vacuum to give the title compound (382 g). The filtrate was concentrated to a residue and suspended in MTBE (100 ml) to give the second crop of the title compound (14.0 g). The total yield was 396 g (90.5%). Mp 138-140° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06743794B2 |
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| 出典データセット | uspto-grants-2004_06 |
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| ORD ID | ord-1a22a9b284944989b8ea87f7105a94c8 |
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| 出典メモ | uspto-grants-2004_06 |
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