تفاعل #75448

ord-301d927b94914e268cbcd3cbef99c291

معادلة التفاعل

CC(C)=CCCBr
5-Bromo-2-methyl-2-pentene
O=C([O-])[O-].[K+].[K+]
K2CO3
O=[N+]([O-])c1ncc[nH]1
2-nitroimidazole
CC(C)=CCCn1ccnc1[N+](=O)[O-]
title product
CC(C)=CCCn1ccnc1[N+](=O)[O-]
4-Methyl-1-(2-nitro-1H-imidazol-1-yl)-3-pentene

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
75°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىDMF was evaporated on a rotary evaporator
  2. 2
    workup.STIRRINGThe yellow gummy residue was stirred with water (150 mL)
  3. 3
    أخرىto give yellow solid, which
  4. 4
    تجفيفdried over Na2SO4
  5. 5
    أخرىevaporated on a rotary evaporator

الإجراء التجريبي

5-Bromo-2-methyl-2-pentene (25 g, 0.154 mol) was dissolved in dry dimethylformamide (DMF) (200 mL). To the solution was added K2CO3 (21.3 g, 0.154 mol) and 2-nitroimidazole (17.4 g, 0.154 mol). The mixture was stirred under N2 atmosphere at 75° C. for 48 hours. DMF was evaporated on a rotary evaporator. The yellow gummy residue was stirred with water (150 mL) to give yellow solid, which was dissolved in diethyl ether (150 mL), dried over Na2SO4 and evaporated on a rotary evaporator to yield the title product. Yield 27.8 g (92%). mp: 49-51° C. MS: (M+H)+=196, M+=195. 1H NMR (CDCl3) δ1.45 and 1.68 (s, 6H, gem-di-CH3), 2.52 (q, 2H, CH2CH═), 4.43 [t, 2H, CH2-(2-nitroimidazolyl)], 5.08 (t, 1H, CH2CH═), 7.05 and 7.14 (s, 2H, 2-nitroimidazolyl-H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06699458B2uspto-grants-2004_03