HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489888Generated: October 23, 2026
9-Anthracenecarboxylic acid → Anthracene-9-carbonyl chloride
https://huagongshe.com/en/reaction/489888
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 9-Anthracenecarboxylic acid | HCID 2201 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | Anthracene-9-carbonyl chloride | HCID 167528 | 59% |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06979741B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-6d6df2e26fae423f9920d14f54d9331b |
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| Source note | uspto-grants-2005_12 |
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