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HRID 55415作成日:2026年10月23日

2-Methoxyphenylacetic acid → (3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-[(2methoxyphenyl)acetyl]-4-perhydroisoindolone

https://huagongshe.com/ja/reaction/55415

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methoxyphenylacetic acidHCID 7134—
反応物TriethylamineHCID 8471—
反応物(3aRS,7SR,7aRS)-7-methyl-7-phenyl-4-perhydroisoindolone hydrochlorideHCID 67713963—
溶媒DichloromethaneHCID 6344—
生成物(3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-[(2methoxyphenyl)acetyl]-4-perhydroisoindoloneHCID 6771403349.5%

反応手順

To a solution of 1.66 g of 2-methoxyphenylacetic acid in 40 cm3 of dichloromethane are added, at 4° C., 1.62 g of N,N'-carbonyldiimidazole. Stirring for 30 minutes at room temperature is followed by dropwise addition of a solution containing 1.85 g of (3aRS,7SR,7aRS)-7-methyl-7-phenyl-4-perhydroisoindolone hydrochloride and 0.7 g of triethylamine in 30 cm3 of dichloromethane. After stirring for 2 hours, the reaction mixture is washed twice with 50 cm3 of water and then with 50 cm3 of saturated aqueous sodium chloride solution. The organic phase is separated out after settling has taken place, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (2.7 kPa). The residue is chromatographed on a column of silica gel (particle size 0.04-0.06 mm, diameter 3 cm, height 15 cm), eluting under a pressure of 0.5 bar of nitrogen with a mixture of cyclohexane and ethyl acetate (80/20 by volume) and collecting 50 cm3 fractions. Fractions 16 to 60 are combined and then concentrated to dryness under reduced pressure (2.5 kPa). The residue is crystallized in 30 cm3 of ethyl acetate. 1.3 g of (3aRS,7SR,7aRS)-7-methyl-7-phenyl-2-[(2-methoxyphenyl)acetyl]-4-perhydroisoindolone are obtained, in the form of white crystals melting at 160° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624950
出典データセットuspto-grants-1997_04
ORD IDord-758961b7be7d45b5a4c2c263c57f103b
出典メモuspto-grants-1997_04