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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423237Generated: October 31, 2026

Benzyl Bromide → Benzyl 2-methoxy-3-nitrobenzoate

https://huagongshe.com/reaction/2423237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methoxy-3-nitrobenzoic acidHCID 12015195—
SolventDimethylformamideHCID 6228—
ProductBenzyl 2-methoxy-3-nitrobenzoateHCID 67246088—

Reaction Steps

At room temperature, benzyl bromide (8.85 mL) and potassium carbonate (10.3 g) were added to a DMF (150 mL) solution of 2-methoxy-3-nitrobenzoic acid (9.80 g), followed by stirring for 70 minutes. The insoluble matter was separated by filtration, followed by evaporation under reduced pressure. This was subjected to liquid-liquid separation with ethyl acetate, aqueous sodium hydrogencarbonate solution, and hexane added thereto. The organic layer was washed with water and saturated brine in that order, dried, and then evaporated under reduced pressure to obtain benzyl 2-methoxy-3-nitrobenzoate (14.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960562B2
Source datasetuspto-grants-2011_06
ORD IDord-75956b4746904735a1e1ff72c34da9c7
Source noteuspto-grants-2011_06