参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 9-蒽甲酸 | HCID 2201 | — |
| 反应物 | 三氯甲烷 | HCID 6212 | — |
| 溶剂 | 氯化亚砜 | HCID 24386 | — |
| 产物 | 9-蒽甲酰氯 | HCID 167528 | 59% |
反应步骤
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.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US06979741B2 |
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| 来源数据集 | uspto-grants-2005_12 |
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| ORD ID | ord-6d6df2e26fae423f9920d14f54d9331b |
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| 来源说明 | uspto-grants-2005_12 |
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