HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586875Generated: November 2, 2026
Potassium Carbonate → HCID 22329202, compound
https://huagongshe.com/reaction/586875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22329270 | HCID 22329270 | — |
| Reactant | HCID 86756825 | HCID 86756825 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | HCID 22329202 | HCID 22329202 | 93.2% |
Reaction Steps
In a mixture of water ethanol toluene (1:1:10, v/v, 42.0 ml) were dissolved 4-(2-propoxy)ethoxyphenyl borate (920 mg) and methyl 7-bromo-1-(t-butoxycarbonyl)-2,3-dihydro-1H-1-benzazepine-4-carboxylate (1308 mg). To the solution was added potassium carbonate (1135 mg), and the mixture was stirred under argon atmosphere at room temperature for 30 minutes. To the mixture was added tetrakistriphenylphosphinepalladium (119 mg), and the mixture was heated to reflux under argon atmosphere for 14.5 hours. The mixture was diluted with ethyl acetate, and washed with water and saturated brine, and the organic layer was dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified with silica gel column chromatography (50 g, hexane:ethyl acetate=9:1→3:1) to give methyl 1-(t-butoxycarbonyl)-7-[4-(2-propoxy)ethoxyphenyl]-2.3-dihydro-1H-1-benzazepine-4-carboxylate (1536 mg, 93%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936602B1 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-8a44390e3d274c4ebbda253c6f4c6630 |
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| Source note | uspto-grants-2005_08 |
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