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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1661962Erstellt: 25. Oktober 2026

Dimethylformamide → HCID 178463133, Verbindung

https://huagongshe.com/reaction/1661962

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktOxalyl chlorideHCID 65578—
Edukt3-(2-Methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acidHCID 66756524—
EduktHCID 178463041HCID 178463041—
LösungsmittelChloroformHCID 6212—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178463133HCID 178463133—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08030498B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-a3cf3055e7084903af2ae88119e9ff15
Quellennotizuspto-grants-2011_10