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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257998Generated: October 25, 2026

Dimethylformamide → HCID 178463133, compound

https://huagongshe.com/reaction/1257998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(2-Methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acidHCID 66756524—
ReactantHCID 178463041HCID 178463041—
SolventChloroformHCID 6212—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 178463133HCID 178463133—

Reaction Steps

To a solution of 3-(2-methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acid (200 mg, 6.90×10−4 mol) in chloroform (15 mL) were added oxalyl chloride (0.5 mL) and DMF in a catalytic amount. The reaction mixture was stirred at room temperature for 30 minutes, and the solvent was distilled off under reduced pressure. The residue was dissolved in anhydrous THF (20 mL), and 5-hydroxy-1-ethylpyrazole hydrochloride (134 mg, 9.01×10−4 mol), triethylamine (139 mg) and N,N-dimethylaminopyridine (170 mg) were added. The mixture was heated at refluxed temperature for 1 hour. The reaction mixture was allowed to cool to room temperature, and then ethyl acetate (200 mL) was added. The mixture was washed twice with a saturated brine, and the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. The residue was dissolved in anhydrous acetonitrile (10 mL), and triethylamine (139 mg) and acetone cyanohydrin in a catalytic amount were added, followed by stirring for 12 hours at room temperature. The solvent was distilled off under reduced pressure to obtain crude 5-hydroxy-1-ethylpyrazol-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-6f829ba4eeb440e79a55d935627b1cb6
Source noteuspto-grants-2013_06