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HRID 6431생성일: 2026년 10월 23일

O-Phenylenediamine → 2-(1H-Pyrrol-2-yl)-1H-benzimidazole

https://huagongshe.com/ko/reaction/6431

반응식

참여 물질

역할이름HCID투입량
반응물O-PhenylenediamineHCID 7243—
반응물Pyrrole-2-Carboxylic AcidHCID 12473—
용매Sodium BicarbonateHCID 516892—
생성물2-(1H-Pyrrol-2-yl)-1H-benzimidazoleHCID 63941927.3%

반응 조건

온도80 °C

반응 단계

A mixture of 1.08 g (10 mmol) of o-phenylenediamine and 20 g of polyophosphate esters was heated gently at 80° C. and was added portionwise 1.11 g (10 mmol) of pyrrole-2-carboxylic acid. After the mixture was stirred at 100° C. for 30 minutes, it was poured into a saturated solution of sodium bicarbonate (500 mL) and stirred until polyphosphate esters was decomposed. It was then extracted with two 400 mL portions of ethyl acetate. the separated organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a crude product. After purification by column chromatography on silica gel with 30% ethyl acetate in hexane, the desired product, 2-(pyrrol-2-yl)benzimidazole (0.50 g, 25%) was obtained as a pale yellow solid, m.p. 250° C.; 1H-NMR (Acetone-d6) 6.25-6.27 (m, 1H, ArH), 6.90-6.92 (m, 1H, ArH), 7.02-7.03 (m, 1H, ArH), 7.14-7.19 (m, 2H, 2xArH), 7.52 (bs, 2H, 2xArH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248782
출처 데이터셋uspto-grants-1993_09
ORD IDord-f133d8b34fb84de6ae33d093fc5b41e4
출처 메모uspto-grants-1993_09