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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
Reactantethyl 5-(4-bromo-2-formyl-N-propylanilino)pentanoateHCID 86595581—
SolventWaterHCID 962—
SolventDimethyl CarbonateHCID 12021—
ProductMethyl 8-bromo-1-propyl-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylateHCID 6865011176.6%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741943B2
Source datasetuspto-grants-2014_06
ORD IDord-d2908c0642ed4894a5c288133d63ddeb
Source noteuspto-grants-2014_06