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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963005Generated: October 28, 2026

Acetonitrile → 2,6-Difluoro-3-methoxybenzonitrile

https://huagongshe.com/reaction/1963005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2,6-Difluoro-3-methoxybenzamideHCID 3544383—
SolventDimethylformamideHCID 6228—
Product2,6-Difluoro-3-methoxybenzonitrileHCID 379183266%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an ice cold solution of DMF (0.45 ml) and acetonitrile (10 ml) was added oxalyl chloride (0.41 g, 0.28 ml, 3.20 mmol) dropwise while maintaining the temperature to 0° C. The reaction mixture was stirred at 0° C. for 40 min followed by addition of a solution of 2,6-difluoro-3-methoxybenzamide (0.50 g, 2.70 mmol) in DMF (4.5 ml).The resulting reaction mixture was stirred at 0° C. 40 min and then allowed to come to room temperature. After completion of reaction (10 min, TLC monitoring), triethyl amine (0.57 g, 0.80 ml, 5.67 mmol) was added dropwise. The reaction mass was concentrated in vacuo followed by addition of water (100 ml) and extraction with ethyl acetate (3×100 ml). The combined organics was washed with water, brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (60-120 M, 10% EtOAc-Hexane) to get the desired product (0.30 g, 66%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415383B2
Source datasetuspto-grants-2013_04
ORD IDord-684e7acc92c545c3ab8af53c5a4710b2
Source noteuspto-grants-2013_04