Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoateHCID 11575669—
SolventWaterHCID 962—
SolventDimethyl CarbonateHCID 12021—
ProductMethyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylateHCID 6865475873.5%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183273B2
Source datasetuspto-grants-2012_05
ORD IDord-4fef573bcb2e4e95b553a141e5c4c2a2
Source noteuspto-grants-2012_05