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HRID 1661962作成日:2026年10月26日

Dimethylformamide → HCID 178463133、化合物

https://huagongshe.com/reaction/1661962

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Oxalyl chlorideHCID 65578—
反応物3-(2-Methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acidHCID 66756524—
反応物HCID 178463041HCID 178463041—
溶媒ChloroformHCID 6212—
溶媒TriethylamineHCID 8471—
溶媒Ethyl AcetateHCID 8857—
生成物HCID 178463133HCID 178463133—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030498B2
出典データセットuspto-grants-2011_10
ORD IDord-a3cf3055e7084903af2ae88119e9ff15
出典メモuspto-grants-2011_10