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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1661962생성일: 2026년 10월 25일

Dimethylformamide → HCID 178463133, 화합물

https://huagongshe.com/reaction/1661962

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물3-(2-Methoxyethoxy)-2-methyl-4-(methylsulfonyl)benzoic acidHCID 66756524—
반응물HCID 178463041HCID 178463041—
용매ChloroformHCID 6212—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물HCID 178463133HCID 178463133—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030498B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-a3cf3055e7084903af2ae88119e9ff15
출처 메모uspto-grants-2011_10