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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1029868생성일: 2026년 10월 27일

Phenylacetic Acid → (3aRS,7aRS)-7,7-diphenyl-2-(phenylacetyl)-4-perhydroisoindolone

https://huagongshe.com/reaction/1029868

반응식

참여 물질

역할이름HCID투입량
반응물Phenylacetic AcidHCID 999—
반응물TriethylamineHCID 8471—
반응물7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochlorideHCID 21264543—
용매DichloromethaneHCID 6344—
생성물(3aRS,7aRS)-7,7-diphenyl-2-(phenylacetyl)-4-perhydroisoindoloneHCID 6791616167%

반응 단계

N,N'-Carbonyldiimidazole (1.7 g) is added to a solution of phenylacetic acid (1.34 g) in dry dichloromethane (30 cc) cooled to +5° C. The mixture is stirred for 1 hour at +5° C. and a solution of 7,7-diphenyl-4-perhydroisoindolone hydrochloride (3.27 g) and triethylamine (1.7 cc) in dichloromethane (30 cc) is then added. The reaction mixture is stirred for 1 hour at +5° C. and then for 1 hour at 20° C. The reaction mixture is washed with a saturated aqueous solution (50 cc) of sodium bicarbonate, dried over magnesium sulphate and filtered and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is crystallized from acetonitrile (15 cc). The crystals are drained, washed with isopropyl ether (10 cc) and dried. (3aRS,7aRS)-7,7-diphenyl-2-(phenylacetyl)-4-perhydroisoindolone (2.7 g) melting at 216° C. is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05102667
출처 데이터셋uspto-grants-1992_04
ORD IDord-5c3ef38f7888458aac459354f47d2c9d
출처 메모uspto-grants-1992_04