HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492197Generated: October 29, 2026
Oxalyl chloride → HCID 86596413, compound
https://huagongshe.com/reaction/492197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 68969741 | HCID 68969741 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86596413 | HCID 86596413 | 115% |
Reaction Steps
0.6 cm3 (6.88 mmol) of oxalyl chloride is added to a suspension, cooled to a temperature in the region of 5° C., of 0.74 g (2.28 mmol) of 3-carboxy-1-(quinol-8-yl)-1H-indole hydrochloride in 15 cm3 of dichloromethane under an argon atmosphere. After stirring at a temperature in the region of 22° C. for 15 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give 0.9 g of 3-chlorocarbonyl-1-(quinol-8-yl)-1H-indole hydrochloride in the form of a yellow solid which is used directly in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531663B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-61c35ab6062b42559d986cfb96c34b20 |
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| Source note | uspto-grants-2009_05 |
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