HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108741Generated: October 29, 2026
2-Chlorobenzoyl chloride → HCID 22627283, compound
https://huagongshe.com/reaction/1108741
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22627421 | HCID 22627421 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22627283 | HCID 22627283 | 115.4% |
Reaction Steps
To a stirred mixture of benzyl 3-isobutyryl-2-propylindole-6-carboxylate (207 mg) and diisopropylethylamine (295 mg) in dichloromethane (6 ml) were added 2-chlorobenzoyl chloride (299 mg) and 4-dimethylaminopyridine (12 mg) at 0° C. The reaction mixture was refluxed for 15 hours. The reaction mixture was cooled to 20° C. and washed with 1N hydrochloric acid, water, saturated sodium bicarbonate, water and brine. The organic phase was dried over sodium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:10) to give benzyl 1-(2-chlorobenzoyl)-3-isobutyryl-2-propylindole-6-carboxylate (330 mg) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06069156 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-b676817f573d48e0a4f88c24529d5791 |
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| Source note | uspto-grants-2000_05 |
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