HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586923Generated: October 26, 2026
Water → methyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate
https://huagongshe.com/reaction/586923
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate | HCID 22328963 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate | HCID 22329080 | — |
Reaction Steps
In DMF (3 ml) was dissolved methyl 7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate (0.3 g), and the solution was added dropwise to a suspension of 60% sodium hydride (0.05 g) in DMF (1 ml) under ice-cooling. The mixture was stirred under nitrogen atmosphere for 10 minutes. Benzyl bromide (0.15 ml) was added thereto, and the mixture was heated at 45° C. for 4 hours. The mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified with silica gel column chromatography (ethyl acetate/hexane) to give methyl 1-benzyl-7-bromo-2,3-dihydro-1H-1-benzazepine-4-carboxylate (0.3 g) as yellow 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-625f389470204eb499acabf1164a22ac |
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| Source note | uspto-grants-2005_08 |
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