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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928542Generated: October 30, 2026

Dimethylformamide → Methyl 3-(benzyloxy)-4-bromo-2-nitrobenzoate

https://huagongshe.com/reaction/928542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-bromo-3-hydroxy-2-nitrobenzoateHCID 58497911—
SolventWaterHCID 962—
ProductMethyl 3-(benzyloxy)-4-bromo-2-nitrobenzoateHCID 2177168597.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of methyl 4-bromo-3-hydroxy-2-nitrobenzoate (5.41 g, 19.6 mmol) and potassium carbonate (5.42 g, 39.2 mmol) in N,N-dimethylformamide (30 mL, 387 mmol) was treated with benzyl bromide (3.26 mL, 27.4 mmol) and stirred at 60° C. for 1 h. The reaction mixture was diluted with water (250 mL) and extracted with ethyl acetate (2×150 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered, and concentrated to give a crude tan oil. Purification by flash column chromatography (100% hexanes to 50% EtOAc/hexanes) gave the desired product (6.99 g, 97%) as a yellow solid. LCMS calculated for C15H16BrN2O5 (M+NH4)+: m/z=383.0, 385.0. found: 383.0, 385.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290514B2
Source datasetuspto-grants-2016_03
ORD IDord-2c0ecb4e5543412c93c153abad1936c2
Source noteuspto-grants-2016_03