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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22396생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Tin tetrachlorideHCID 24287—
반응물2-Thiophenecarbonyl chlorideHCID 78928—
반응물2-(1H-Pyrrol-1-yl)isoindoline-1,3-dioneHCID 853719—
용매DichloromethaneHCID 6344—
생성물2-[2-(2-thienylcarbonyl)-1H-pyrrol-1-yl]-1H-isoindole-1,3(2H)dioneHCID 19973158—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428053
출처 데이터셋uspto-grants-1995_06
ORD IDord-f39d34e49ba848f1a443ec206f20e892
출처 메모uspto-grants-1995_06