HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402260Generated: October 30, 2026
Hydrochloric Acid → Methyl 8-bromo-1-propyl-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylate
https://huagongshe.com/reaction/402260
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | ethyl 5-(4-bromo-2-formyl-N-propylanilino)pentanoate | HCID 86595581 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethyl Carbonate | HCID 12021 | — |
| Product | Methyl 8-bromo-1-propyl-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylate | HCID 68650111 | 76.6% |
Reaction Steps
To a solution of ethyl 5-(4-bromo-2-formyl-N-propylanilino)pentanoate (5.0 g) in dimethylcarbonate (100 ml) was added a methanol solution of 28% sodium methoxide (3.5 g), and the mixture was heated at 50° C. for 2 hours under a nitrogen atmosphere. After cooling to 0° C. and neutralization with 1N hydrochloric acid, to the solution was added water, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline, and dried over magnesium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1) to obtain yellow oil of methyl 8-bromo-1-propyl-1, 2, 3,4-tetrahydro-1-benzazocine-5-carboxylate (3.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741943B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-d2908c0642ed4894a5c288133d63ddeb |
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| Source note | uspto-grants-2014_06 |
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