関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | O-Phenylenediamine | HCID 7243 | — |
| 反応物 | Pyrrole-2-Carboxylic Acid | HCID 12473 | — |
| 溶媒 | Sodium Bicarbonate | HCID 516892 | — |
| 生成物 | 2-(1H-Pyrrol-2-yl)-1H-benzimidazole | HCID 639419 | 27.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05248782 |
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| 出典データセット | uspto-grants-1993_09 |
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| ORD ID | ord-f133d8b34fb84de6ae33d093fc5b41e4 |
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| 出典メモ | uspto-grants-1993_09 |
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