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HRID 6431作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物O-PhenylenediamineHCID 7243—
反応物Pyrrole-2-Carboxylic AcidHCID 12473—
溶媒Sodium BicarbonateHCID 516892—
生成物2-(1H-Pyrrol-2-yl)-1H-benzimidazoleHCID 63941927.3%

反応条件

温度80 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248782
出典データセットuspto-grants-1993_09
ORD IDord-f133d8b34fb84de6ae33d093fc5b41e4
出典メモuspto-grants-1993_09