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HRID 22396作成日:2026年10月24日

Tin tetrachloride → 2-[2-(2-thienylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dione

https://huagongshe.com/ja/reaction/22396

反応式

関与物質

役割名称HCID仕込み量
反応物Tin tetrachlorideHCID 24287—
反応物2-Thiophenecarbonyl chlorideHCID 78928—
反応物2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
溶媒DichloromethaneHCID 6344—
生成物2-[2-(2-thienylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dioneHCID 19973158—

反応手順

A solution of 2-thiophenecarbonylchloride (10.7 ml) in 500 ml of dry DCM was treated at -10° C. with tin tetrachloride (11.7 ml) and stirred for 30 minutes. 2-(1H-pyrrol-1-yl)-1H-isoindole-1,3(2H)dione (21.2 g) was then added in small portions over a period of 30 minutes at -10° C. After the addition was completed, the reaction mixture was stirred for an additional 30 minutes at -10° C. and subsequently poured into 500 ml of ice water. The precipitate was dissolved by addition of about 1000 ml of DCM and the separated aqueous layer extracted again with DCM. The combined organic layers were washed twice with 2N hydrochloric acid and with water, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by flash column chromatography (silica gel, DCM/ethyl acetate 99:1) and the desired fractions were concentrated. The residue was recrystallized from DCM/ethyl ether affording the product as crystals (17.9 g), m.p. 165°-166° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428053
出典データセットuspto-grants-1995_06
ORD IDord-f39d34e49ba848f1a443ec206f20e892
出典メモuspto-grants-1995_06