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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405070Generated: November 1, 2026

Potassium Carbonate → 1-Bromo-2-(2-fluoroethoxy)-4-nitrobenzene

https://huagongshe.com/reaction/1405070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Fluoroethyl bromideHCID 12982—
Reactant2-Bromo-5-nitrophenolHCID 12867136—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Bromo-2-(2-fluoroethoxy)-4-nitrobenzeneHCID 86720061—

Reaction Conditions

Temperature100 °C

Reaction Steps

Intermediate 16A (475 mg, 2.179 mmol) was dissolved in DMF (1 mL) and to this solution was added potassium carbonate (903 mg, 6.54 mmol) and 1-bromo-2-fluoroethane (415 mg, 3.27 mmol). The reaction mixture was stirred at 100° C. for 3 hours, cooled, diluted with water (20 mL) and then extracted with EtOAc (2×20 mL). The combined organics were washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Intermediate 16B was obtained as a pale yellow semi-solid (570 mg, 2.159 mmol, 99% yield). MS (ES): m/z=199.0 [M+H]+. 1H NMR (400 MHz, DMSO-d6) δ ppm 4.47-4.51 (m, 1 H) 4.55-4.59 (m, 1 H) 4.73-4.78 (m, 1 H) 4.85-4.91 (m, 1 H) 7.77-7.83 (m, 1 H) 7.91 (d, J=2.51 Hz, 1 H) 7.94 (d, J=8.53 Hz, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916553B2
Source datasetuspto-grants-2014_12
ORD IDord-c95b2733945f4917937735563fd14e6a
Source noteuspto-grants-2014_12