HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928939Generated: October 29, 2026
Hydrochloric Acid → Methyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylate
https://huagongshe.com/reaction/1928939
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoate | HCID 11575669 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethyl Carbonate | HCID 12021 | — |
| Product | Methyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylate | HCID 68654758 | 73.5% |
Reaction Steps
To a solution of methyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoate (45.7 g) in dimethyl carbonate (900 ml) was added a methanol solution of sodium methoxide (28%, 26.4 g) and then the mixture was stirred at 50° C. under nitrogen atmosphere for 6 hours. The resultant was cooled to 0° C., followed by addition of water, neutralized with 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was recrystallized from hexane-ethyl acetate to give methyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-terahydro-1-benzoazocine-5-carboxylate (32.2 g) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183273B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-4fef573bcb2e4e95b553a141e5c4c2a2 |
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| Source note | uspto-grants-2012_05 |
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