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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502019Generated: October 30, 2026

Ethanol → HCID 86727069, compound

https://huagongshe.com/reaction/1502019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3-Bromo-6-fluoro-2-methoxybenzonitrileHCID 71270710—
CatalystHCID 178418807HCID 178418807—
ProductHCID 86727069HCID 86727069—

Reaction Steps

3-bromo-6-fluoro-2-methoxybenzonitrile (4.40 g, 19.1 mmol), potassium vinyl trifluoroborate (5.12 g, 38.3 mmol), PdCl2(dppf)-CH2Cl2 Adduct (0.7 g, 1 mmol) and TEA (5.33 mL, 38.3 mmol) were added to 80 mL ethanol in a 200 mL flask. The reaction mixture was degassed and heated to reflux for 4 h. The reaction mixture was cooled and then most of the ETOH was removed. The residue was diluted with ethyl acetate. The mixture was washed with brine twice. The organic layer was separated and dried over Na2SO4, filtered, and evaporated to dryness. The residue was purified thru a 330 g RediSep column and eluted with 10% ETOAc/hexane solvent system to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-a8d12e80008641659734bc3e35d009c7
Source noteuspto-grants-2015_12