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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901869Generated: October 26, 2026

Potassium Acetate → 2-Bromo-6-nitrobenzyl Acetate

https://huagongshe.com/reaction/901869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
Reactant1-Bromo-2-(bromomethyl)-3-nitrobenzeneHCID 15063170—
SolventDimethylformamideHCID 6228—
Product2-Bromo-6-nitrobenzyl AcetateHCID 5882412298.1%

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 ml) 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 numberUS07365063B2
Source datasetuspto-grants-2008_04
ORD IDord-bb5bfffc647e4565b82f7b6047c24c57
Source noteuspto-grants-2008_04