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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295933Generated: October 30, 2026

Benzyl Bromide → 4-Benzyl 1-methyl 2-aminoterephthalate

https://huagongshe.com/reaction/1295933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 21924002HCID 21924002—
SolventDimethylformamideHCID 6228—
Product4-Benzyl 1-methyl 2-aminoterephthalateHCID 1077947770%

Reaction Steps

After dissolving 1-methyl 2-aminoterephthalate (8.00 g, 41.1 mmol) in dimethylformamide (80 ml), anhydrous potassium carbonate (6.25 g, 45.1 mmol) and benzyl bromide (4.12 ml, 43.1 mmol) were added and the mixture was stirred at room temperature for 15.5 hours. An excess of triethylamine was added, and after stirring for an additional 10 minutes at room temperature, ice water was added and extraction was performed with ethyl acetate. The ethyl acetate layer was washed with water and brine and then dried over anhydrous magnesium sulfate. Filtration was performed with silica gel-alumina and the solvent was distilled off under reduced pressure. IPE was added to the obtained oil for crystallization, and the crystals were filtered off. The filtrate was concentrated and then the same procedure was repeated twice to yield the title compound (8.21 g) as a light yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244730B2
Source datasetuspto-grants-2007_07
ORD IDord-25ee629f8619407fa5451b5545725971
Source noteuspto-grants-2007_07