돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 726713생성일: 2026년 10월 24일

Dimethyl Sulfoxide → 1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanal

https://huagongshe.com/ko/reaction/726713

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물2-(4-hydroxybutyl)-1H-Isoindole-1,3(2H)-dioneHCID 11117528—
용매DichloromethaneHCID 6344—
생성물1,3-Dihydro-1,3-dioxo-2H-isoindole-2-butanalHCID 7715082.8%

반응 조건

온도-78 °C

반응 단계

Oxalyl Chloride (4.01 ml; 46 mmol) in 90 ml dichloromethane was cooled at -78° C. in a dry ice-acetone bath. Dimethylsulfoxide (4.26 ml; 60 mmol) in 22 ml dichloromethane was then added dropwise and the mixture stirred at -78° C. for 30 minutes. N-(4-Hydroxybutyl)phthalimide (9.108 g; 41.5 mmol) in 45 ml dichloromethane was then added and the mixture stirred in the -78° C. bath for 45 minutes. The mixture was then warmed in a 0° C. ice bath and stirred for one hour. Triethylamine (23 g; 230 mmol) in 23 ml dichloromethane was then added and the stirred for an additional 30 minutes. The mixture was worked up by washing with water. The organic layer was separated, dried (MgSO4), filtered, concentrated and the residue purified by flash chromatography; 200 g silica gel column using 1:3 ethyl acetate:Hexane to provide N-(4-oxobutyl)phthalimide as a white solid (7.469 g; 82.8% yield). 1 H NMR (300 MHz, CDCl3): 2.023 (m, 2H); 2.546 (dt, 2H, J1 =7.324 Hz, J2 =1.098 Hz); 3.749 (t, 2H, J=6.958 Hz); 7.734 (m, 2H); 7.845 (m, 2H); 9.777 (t, 1H, J=1.099 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05710159
출처 데이터셋uspto-grants-1998_01
ORD IDord-882f43c3752d4cfaa7db48613ec305ff
출처 메모uspto-grants-1998_01