関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 9-Anthracenecarboxylic acid | HCID 2201 | — |
| 反応物 | Chloroform | HCID 6212 | — |
| 溶媒 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | Anthracene-9-carbonyl chloride | HCID 167528 | 59% |
反応手順
Anthracene-9-carboxylic acid (recrystallized from ethanol, 12.05 g, 54.3 mmol) was suspended in a mixture of chloroform (60 mL, Aldrich, amylenes-stabilized) and thionyl chloride (12 mL) and heated under reflux until a clear solution was obtained (about 30 minutes). The solvent was removed by distillation under reduced pressure and the residual hot oil was dissolved in toluene (20 mL) and hexane (100 mL) was added. After cooling to ambient temperature the crystalline product was collected by filtration and dried in a stream of nitrogen then under high vacuum to give the title compound as a yellow solid (7.69 g, 59%). Non-commercially available carboxylic acids referred to in this section were prepared as described below. If desired they were converted to the corresponding carbonyl chloride using thionyl chloride as described above.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06979741B2 |
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| 出典データセット | uspto-grants-2005_12 |
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| ORD ID | ord-6d6df2e26fae423f9920d14f54d9331b |
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| 出典メモ | uspto-grants-2005_12 |
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