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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1029876생성일: 2026년 10월 26일

Triethylamine → (3aRS,7aRS)-2-[(2,6-difluorophenyl)acetyl]-7,7-diphenyl-4-perhydroisoindolone

https://huagongshe.com/reaction/1029876

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2,6-Difluorophenylacetic acidHCID 123585—
반응물7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochlorideHCID 21264543—
용매DichloromethaneHCID 6344—
생성물(3aRS,7aRS)-2-[(2,6-difluorophenyl)acetyl]-7,7-diphenyl-4-perhydroisoindoloneHCID 6791605367.6%

반응 단계

N,N'-Carbonyldiimidazole (1.13 g) is added to a solution of 2-(2,6-difluorophenyl)acetic acid (1.2 g) in dry dichloromethane (30 cc), cooled to +5° C. The mixture is stirred for 45 minutes at +5° C. and a solution of (3aRS,7aRS)-7,7-diphenyl-4-perhydroisoindolone hydrochloride (2.3 g) and triethylamine (0.98 cc) in dichloromethane (40 cc) is then added. The reaction mixture is stirred at 20° C. for 16 hours, then washed with distilled water (2×50 cc), dried over magnesium sulphate and filtered and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized from ethyl acetate (10 cc). The crystals obtained are drained, washed with isopropyl ether (10 cc) and dried. (3aRS,7aRS)-2-[(2,6-difluorophenyl)acetyl]-7,7-diphenyl-4-perhydroisoindolone (2.1 g) melting at 218° C. is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05102667
출처 데이터셋uspto-grants-1992_04
ORD IDord-9ab419e893b24617b15522ad16424269
출처 메모uspto-grants-1992_04