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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1771761생성일: 2026년 10월 26일

Oxalyl chloride → 2-Fluoro-5-(3-fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-3-methyl-benzamide

https://huagongshe.com/reaction/1771761

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물Sodium BicarbonateHCID 516892—
반응물3-Amino-2,4-dimethylphenolHCID 14130608—
반응물2-Fluoro-5-(3-fluorophenyl)-3-methyl-benzoic acidHCID 89443658—
촉매DimethylformamideHCID 6228—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물2-Fluoro-5-(3-fluorophenyl)-N-(3-hydroxy-2,6-dimethyl-phenyl)-3-methyl-benzamideHCID 8944434234%

반응 단계

To a solution of 2-fluoro-5-(3-fluorophenyl)-3-methyl-benzoic acid (intermediate III(f)) (597 mg, 2.41 mmol, 1.1 eq) in CH2Cl2 (15 mL) and DMF (5 drops) was added (COCl)2 (916 mg, 7.22 mmol, 3.3 eq) at 0° C. The reaction mixture was stirred at room temperature for 1.5 h. The resulting mixture was concentrated under reduced pressure to remove the solvent and excess reagent and the residue obtained dissolved in THF (20 mL) and added dropwise to a solution of 3-amino-2,4-dimethylphenol (intermediate X(c)) (300 mg, 2.18 mmol, 1.0 eq) and NaHCO3 (920 mg, 10.9 mmol, 5 eq) in THF (20 mL) at 0° C. After the addition was completed, the reaction mixture was stirred at room temperature for 1 h. Water was added and the aqueous layer extracted with EtOAc. The organic extract was washed with water and brine, dried (Na2SO4), filtered, and evaporated in vacuo. The residue was purified by column chromatography (CH2Cl2:MeOH, 500:1 to 300:1) to give the title compound as a white solid (270 mg, 34%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09249085B2
출처 데이터셋uspto-grants-2016_02
ORD IDord-c2d3db5c991f44b790956f8ad225e1c9
출처 메모uspto-grants-2016_02