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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361633Generated: October 30, 2026

p-Fluoronitrobenzene → 4,4,5,5-Tetramethyl-2-(2-(4-nitrophenoxy)phenyl)-1,3,2-dioxaborolane

https://huagongshe.com/reaction/1361633

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenolHCID 2734622—
SolventDimethylformamideHCID 6228—
Product4,4,5,5-Tetramethyl-2-(2-(4-nitrophenoxy)phenyl)-1,3,2-dioxaborolaneHCID 66731681—

Reaction Steps

To a solution of 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol (2.00 g, 9.09 mmol) in DMF was added Potassium carbonate (2.51 g, 18.2 mmol) and 1-fluoro-4-nitrobenzene (0.964 ml, 9.09 mmol). The reaction was flushed with nitrogen, sealed, and heated to 120 deg.C. After 18 h, water was added and the mixture extracted twice with EtOAc. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. Purify by silica gel chromatography, eluting with 0-15% EtOAc/hexanes to give 4,4,5,5-tetramethyl-2-(2-(4-nitrophenoxy)phenyl)-1,3,2-dioxaborolane as a white solid. MS m/z=342 [M+1]+. Calc'd for C18H20BNO5: 341.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880000B2
Source datasetuspto-grants-2011_02
ORD IDord-e04830de52484e4cb229f4bf03c30ad6
Source noteuspto-grants-2011_02