HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608930Generated: October 29, 2026
Potassium Carbonate → HCID 54369859, compound
https://huagongshe.com/reaction/1608930
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Benzene, 4-bromo-1,2-dimethoxy- | HCID 76114 | — |
| Reactant | HCID 47169039 | HCID 47169039 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 54369859 | HCID 54369859 | — |
Reaction Steps
4-Bromoveratrole (5.7 g, 26 mmol), 6-chloroindole-2-carboxylic acid morpholide (1.7 g, 6.5 mmol), potassium carbonate (1.7 g), copper(I) bromide (0.2 g) in a mixture of pyridine (2 ml) and nitrobenzene was stirred at 140° C. for 14 hours. After cooling to room temperature, the reaction mixture was applied onto a flash chromatography column (silica gel, 140 g), Elution with toluene, toluene/acetone [9:1] and toluene/acetone [8:2] (500 ml each) gave 6-chloro-1-(3,4-dimethoxyphenyl)indole-2-carboxylic acid morpholide as brown oil. Yield: 2.1 g (81% of theoretical) Rf : 0.54 (toluene/acetone, 7:3). The H-NMR spectra was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05399559 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-a33721e21b704016928abe57b8007dfb |
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| Source note | uspto-grants-1995_03 |
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