돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239992생성일: 2026년 10월 25일

Triethylamine → Methyl 4-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoate

https://huagongshe.com/reaction/239992

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Propylphosphonic anhydrideHCID 111923—
반응물Benzoic acid, 4-amino-3,5-dimethyl-, methyl esterHCID 11030398—
반응물5-Bromo-2-trifluoromethylbenzoic acidHCID 50998140—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Methyl 4-[[5-bromo-2-(trifluoromethyl)benzoyl]amino]-3,5-dimethyl-benzoateHCID 8670737840.2%

반응 단계

To a solution of 5-bromo-2-(trifluoromethyl)benzoic acid (1.00 g, 0.00371 mol) in CH2Cl2 (15 mL) at room temperature are added methyl 4-amino-3,5-dimethylbenzoate (0.46 g, 0.00260 mol, see preparation 12) and triethylamine (1.10 ml, 0.00743 mol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 6.00 ml, 0.00929 mol) is added via syringe and stirred at room temperature. After 14 hours, the reaction mixture is diluted with water and extracted with dichloromethane. The organic layers are combined and dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) with 10-15% EtOAc to give the title compound as an off-white solid (0.45 g, 27.67%). Mass spectrum (m/z): 430.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642768B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-2654c8363252447cad4e00376b45a8cf
출처 메모uspto-grants-2014_02