HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587037Generated: November 2, 2026
Water → Methyl 1-isobutyl-7-[4-(2-propoxyethoxy)phenyl]-2,3-dihydro-1-benzazepine-4-carboxylate
https://huagongshe.com/reaction/587037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 7-bromo-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxylate | HCID 22328913 | — |
| Reactant | 4-(2-Propoxyethoxy)phenyl borate | HCID 86756814 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol toluene water | HCID 86587398 | — |
| Product | Methyl 1-isobutyl-7-[4-(2-propoxyethoxy)phenyl]-2,3-dihydro-1-benzazepine-4-carboxylate | HCID 22329296 | 67.9% |
Reaction Steps
In toluene/ethanol/water (=10/1/1, 41 ml) was dissolved methyl 7-bromo-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxylate (0.90 g). To the solution were added 4-(2-propoxyethoxy)phenyl borate (0.72 g) and potassium carbonate (0.81 g) and the mixture was stirred for 30 minutes under argon atmosphere. To the mixture was added tetrakistriphenylphosphinepalladium (123 mg) and the mixture was heated to reflux for 14 hours. After cooling to room temperature, the solution was added to water, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried with magnesium sulfate. The solvent was removed under reduced pressure, and the resulting residue was purified with silica gel column chromatography (hexane/ethyl acetate=8/1) to give methyl 1-isobutyl-7-[4-(2-propoxyethoxy)phenyl]-2,3-dihydro-1-benzazepine-4-carboxylate (0.79 g).
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-0a1d144b11de420f8ba0ec523acbc51a |
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| Source note | uspto-grants-2005_08 |
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