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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257996Generated: October 25, 2026

Dimethylformamide → HCID 178496176, compound

https://huagongshe.com/reaction/1257996

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(2-Methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acidHCID 66756524—
ReactantHCID 178478934HCID 178478934—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 178496176HCID 178496176—

Reaction Steps

To a solution of 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acid (195 mg, 6.76 mmol) in chloroform (15 mL) were added oxalyl chloride (0.5 mL) and DMF in a catalytic amount. The reaction mixture was stirred for 30 minutes at room temperature, and the solvent was distilled off under reduced pressure. The residue was dissolved in anhydrous THF (20 mL), and 5-hydroxy-1-methylpyrazole hydrochloride (136 mg, 1.01 mmol), triethylamine (136 mg) and N,N-dimethylaminopyridine (250 mg) were added, followed by reflux with heating for 1 hour. The reaction mixture was allowed to cool to room temperature, and diluted with ethyl acetate (200 mL). The mixture was washed twice with a saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was dissolved in anhydrous acetonitrile (10 mL), and triethylamine (136 mg) and acetone cyanohydrin in a catalytic amount were added. The mixture was stirred for 12 hours at room temperature. The solvent was distilled off under reduced pressure to obtain crude 5-hydroxy-1-methylpyrazol-4-yl 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)phenyl ketone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466088B2
Source datasetuspto-grants-2013_06
ORD IDord-fc4b8129fba6413ba806cd545a5a8515
Source noteuspto-grants-2013_06