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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928940Generated: November 1, 2026

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

https://huagongshe.com/reaction/1928940

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 numberUS08183273B2
Source datasetuspto-grants-2012_05
ORD IDord-7ad61db351194b358a630d41ef563d8d
Source noteuspto-grants-2012_05