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HRID 375492作成日:2026年10月25日

2-Methoxyphenylacetic acid → (4aRS,7aRS)-4,4-diphenyl-6-[(2-methoxyphenyl)acetyl]perhydrothiopyrano[2,3-c]pyrrole

https://huagongshe.com/reaction/375492

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(4aRS,7aRS)4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole hydrochlorideHCID 67745331—
溶媒DichloromethaneHCID 6344—
生成物(4aRS,7aRS)-4,4-diphenyl-6-[(2-methoxyphenyl)acetyl]perhydrothiopyrano[2,3-c]pyrroleHCID 6774534692.6%

反応条件

温度0 °C

反応手順

1.13 g of N,N'-carbonyldiimidazole are added to a solution, cooled to 0° C., of 1.16 g of 2-methoxyphenylacetic acid in 20 cm3 of dry dichloromethane. The mixture is stirred for 40 minutes at 0° C. and then a solution of 2.15 g of (4aRS,7aRS)4,4-diphenylperhydrothiopyrano[2,3-c]pyrrole hydrochloride and 0.9 cm3 of triethylamine in 20 cm3 of dichloromethane is added. The reaction mixture is stirred for one hour at 0° C. and is then washed with a saturated aqueous solution of sodium hydrogen carbonate. The organic phase is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The solid obtained is washed with 30 cm3 of ethyl ether and 30 cm3 of diisopropyl oxide and it is then dried under reduced pressure (2.7 kPa). 2.66 g of (4aRS,7aRS)-4,4-diphenyl-6-[(2-methoxyphenyl)acetyl]perhydrothiopyrano[2,3 -c]pyrrole are obtained in the form of a white solid; melting point 172° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05484942
出典データセットuspto-grants-1996_01
ORD IDord-2680172248a14bcda158531c8b039243
出典メモuspto-grants-1996_01