تفاعل #6527

ord-f133d8b34fb84de6ae33d093fc5b41e4

معادلة التفاعل

Nc1ccccc1N
o-phenylenediamine
O=C(O)c1ccc[nH]1
pyrrole-2-carboxylic acid
c1c[nH]c(-c2nc3ccccc3[nH]2)c1
2-(pyrrol-2-yl)benzimidazole
المردود 27.3%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصIt was then extracted with two 400 mL portions of ethyl acetate
  2. 2
    تجفيفthe separated organic layer was dried over anhydrous sodium sulfate
  3. 3
    تركيزconcentrated under reduced pressure
  4. 4
    أخرىto give a crude product
  5. 5
    أخرىAfter purification by column chromatography on silica gel with 30% ethyl acetate in hexane

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05248782uspto-grants-1993_09