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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459795Generated: October 26, 2026

Potassium Acetate → 2-Bromo-6-nitrobenzyl Acetate

https://huagongshe.com/reaction/459795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant1-Bromo-2-(bromomethyl)-3-nitrobenzeneHCID 15063170—
SolventDimethylformamideHCID 6228—
Product2-Bromo-6-nitrobenzyl AcetateHCID 58824122—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1-bromo-2-bromomethyl-3-nitro-benzene (3.39 g, 11.53 mmol) in DMF (50 nml) was added KOAc (7.6 g, 77.4 mmol). The reaction was heated at 70° C. for an hour. After cooling to room temperature, the mixture was partitioned between water and ethyl acetate. The organic layer was washed with water and brine, and dried over MgSO4 Acetic acid 2-bromo-6-nitro-benzyl ester (3.1 g) was obtained as a brown oil after concentration under vacuum (˜100%). 1H NMR (CDCl3, 300 MHz) δ: 2.06(s, 3H), 5.46 (s, 2H), 7.377(t, J=8.1 Hz), 7.778(dd, J=1.23 Hz, 8.14 Hz), 7.856(dd, J=1.23 Hz, 8.07 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196087B2
Source datasetuspto-grants-2007_03
ORD IDord-2b245187379b4f5c91e535abb54e0584
Source noteuspto-grants-2007_03