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HRID 1029876作成日:2026年10月27日

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

https://huagongshe.com/reaction/1029876

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,6-Difluorophenylacetic acidHCID 123585—
反応物7,7-Diphenylhexahydro-1H-isoindol-4(2H)-one hydrochlorideHCID 21264543—
溶媒DichloromethaneHCID 6344—
生成物(3aRS,7aRS)-2-[(2,6-difluorophenyl)acetyl]-7,7-diphenyl-4-perhydroisoindoloneHCID 6791605367.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05102667
出典データセットuspto-grants-1992_04
ORD IDord-9ab419e893b24617b15522ad16424269
出典メモuspto-grants-1992_04