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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402270Generated: October 30, 2026

Trifluoroacetic acid → Methyl 8-bromo-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylate

https://huagongshe.com/reaction/402270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylateHCID 68654758—
SolventTolueneHCID 1140—
ProductMethyl 8-bromo-1,2,3,4-tetrahydro-1-benzazocine-5-carboxylateHCID 6865013392.6%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of methyl 8-bromo-1-(4-methoxybenzyl)-1,2,3,4-terahydro-1-benzoazocine-5-carboxylate (10.0 g), in toluene (50 ml) was added trifluoroacetic acid (50 ml), and the mixture was stirred at 65° C. for 2 hours. After distilling off the solvent under reduced pressure, water was added at 0° C. and the reaction mixture was neutralized with potassium carbonate and extracted with ethyl acetate. The organic layer was washed with aqueous saturated sodium bicarbonate solution and saturated brine, after which it was dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by basic silica gel column chromatography (hexane:ethyl acetate=9:1). The resulting solid was washed with hexane to give methyl 8-bromo-1,2,3,4-terahydro-1-benzoazocine-5-carboxylate (6.59 g) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741943B2
Source datasetuspto-grants-2014_06
ORD IDord-d0bea485085a47e88c32ff8fba51830e
Source noteuspto-grants-2014_06