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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911255Generated: October 30, 2026

2-Fluorophenol → HCID 28411324, compound

https://huagongshe.com/reaction/911255

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluorophenolHCID 9707—
ReactantCesium carbonateHCID 10796—
ReactantBenzonitrile, 4-bromo-HCID 12162—
Reactant2,2,6,6-Tetramethyl-3,5-heptanedioneHCID 70700—
CatalystCuprous chlorideHCID 62652—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 28411324HCID 2841132466.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

Mix under argon atmosphere 4-bromobenzonitrile (2.0 g, 11.3 mmol), 2-fluorophenol (2.5 g, 22.6 mmol), 2,2,6,6-tetramethylheptane-3,5-dione (203 mg, 1.1 mmol), and cesium carbonate (7.4 g, 22.6 mmol) in anhydrous NMP (19 mL). Degas the flask, fill with argon and add copper(I) chloride (554 mg, 5.6 mmol) quickly. Degas the flask then fill with argon and heat at 120° C. for 3 h. Cool to ambient temperature, dilute with EtOAc, filter and wash the filtrate sequentially with 2M aqueous HCl, 0.3M aqueous HCl, 2M aqueous NaOH and brine. Separate the organic layer, dry over Na2SO4 and concentrate in vacuo. Purify by chromatography on silica gel eluting with hexane/EtOAc (1:0 and 9:1) to obtain the desired intermediate (1.6 g, 66%). MS (ES+) m/z: 231 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-05eb2bdf9bda4564b279fd29229ba0f4
Source noteuspto-grants-2011_09