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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1191680Generated: October 31, 2026

Potassium Carbonate → Methyl 3-(2-tert-butyl-5-methoxyindol-1-ylmethyl)benzoate

https://huagongshe.com/reaction/1191680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromomesityleneHCID 68473—
ReactantMethyl 3-{[2-(2-hydroxy-3,3-dimethylbutyl)-4-methoxyphenylamino]methyl}benzoateHCID 69670829—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(2-tert-butyl-5-methoxyindol-1-ylmethyl)benzoateHCID 6967106967.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a suspension of methyl 3-{[2-(2-hydroxy-3,3-dimethylbutyl)-4-methoxyphenylamino]methyl}benzoate (200 mg), 2-bromomesitylene (0.097 mL) and potassium carbonate (148 mg) in N,N-dimethylformamide (5 mL) was added tetrakis(triphenylphosphine)palladium (0) (31.1 mg) at room temperature, and this resulting mixture was stirred at 150° C. for 2 hours under an argon atmosphere. The reaction mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (127 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680120B2
Source datasetuspto-grants-2014_03
ORD IDord-4ceb0995bed345b08b356f3cb4b8bb01
Source noteuspto-grants-2014_03