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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966375Generated: October 29, 2026

Pinacol → 2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

https://huagongshe.com/reaction/1966375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPinacolHCID 6425—
Reactant(4-Cyano-3-fluorophenyl)boronic acidHCID 2783130—
SolventCyclohexaneHCID 8078—
Product2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 5135095185.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of the crude 3-fluoro-4-cyanophenyl boronic acid (9.2 Kg, 55.8 mol) in cyclohexane (150 L) was treated with pinacol (13.2 Kg, 111.6 mol, 2.0 equiv) at room temperature, and the resulting reaction mixture was warmed to 40° C. for 4 h. When TLC and LC/MS showed that the reaction was deemed complete, the reaction mixture was cooled down to room temperature before being washed with water (2×75 L). The organic layer was then dried over magnesium sulfate (MgSO4) and concentrated under the reduced pressure to afford 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (19, 11.8 Kg, 13.8 Kg theoretical, 85.6% yield) as a light yellow solid. For 19: 1H NMR (300 MHz, DMSO-d6) δ ppm 7.92 (t, 1H, J=7.00 Hz), 7.62 (m, 2H), 1.29 (s, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420645B2
Source datasetuspto-grants-2013_04
ORD IDord-a73efb89defc469a8a93190323f88c12
Source noteuspto-grants-2013_04