돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21006생성일: 2026년 10월 23일

Dimethylformamide → 4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone

https://huagongshe.com/ko/reaction/21006

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물N,N,N',N'-TetramethylethylenediamineHCID 8037—
반응물3-chloro-N-(1-methyl-1-phenylethyl)benzamideHCID 47444761—
반응물HCID 178444656HCID 178444656—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물4-Chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinoneHCID 6849004389%

반응 단계

3-Chloro-N-(1-methyl-1-phenylethyl)benzamide (7.00 g, 25.6 mmol) was dissolved in THF (280 mL), and the solution was added with TMEDA (12.4 mL, 81.9 mmol), then added with sec-butyllithium-hexane solution (0.99 mol/L, 82.7 mL, 81.9 mmol) by drops at −78° C. for 40 minutes under argon atmosphere, followed by stirring at the same temperature for 2.5 hours. Then, the mixture was added with DMF (4.36 mL, 56.3 mmol) and warmed from −78° C. to room temperature over 2 hours. The reaction mixture was added with water, extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by slurry using diisopropyl ether to obtain 4-chloro-3-hydroxy-2-(1-methyl-1-phenylethyl)isoindolinone (6.86 g, yield 89%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745641B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f45e4ddcaba84c37bb2475ecd5f8e92f
출처 메모uspto-grants-2010_06