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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928950Generated: November 1, 2026

Trifluoroacetic acid → methyl 9-bromo-2,3,4,5-tetrahydro-1H-1-benzoazonin-6-carboxylate

https://huagongshe.com/reaction/1928950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantmethyl 9-bromo-1-(4-methoxybenzyl)-2,3,4,5-tetrahydro-1H-1-benzoazonin-6-carboxylateHCID 68650162—
SolventTolueneHCID 1140—
Productmethyl 9-bromo-2,3,4,5-tetrahydro-1H-1-benzoazonin-6-carboxylateHCID 6864985282.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 9-bromo-1-(4-methoxybenzyl)-2,3,4,5-tetrahydro-1H-1-benzoazonin-6-carboxylate (12.5 g) in toluene (62.5 ml) was added trifluoroacetic acid (62.5 ml) and the mixture was stirred under nitrogen atmosphere at 80° C. for 7 hours. After distilling off the solvent under reduced pressure, water was added at 0° C. and the mixture was neutralized with potassium carbonate, and extracted with ethyl acetate. After washing the organic layer with aqueous saturated sodium bicarbonate solution and saturated brine, the resultant was dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate=9:1) and recrystallized from hexane:ethyl acetate to give methyl 9-bromo-2,3,4,5-tetrahydro-1H-1-benzoazonin-6-carboxylate (7.4 g) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183273B2
Source datasetuspto-grants-2012_05
ORD IDord-408148956afe4a7fba43b9d0c53cd429
Source noteuspto-grants-2012_05