تفاعل #172402

ord-48a81b494967407ca32565a61606b854

معادلة التفاعل

Cl
hydrochloric acid
CC(C)(C)[O-].[K+]
potassium tert-butoxide
COc1ccc[nH]c1=O
3-methoxypyridin-2(1H)-one
Cc1cc([N+](=O)[O-])ccc1F
1-fluoro-2-methyl-4-nitrobenzene
COc1cccn(-c2ccc([N+](=O)[O-])cc2C)c1=O
3-Methoxy-1-(2-methyl-4-nitrophenyl)pyridin-2(1H)-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe reaction solution is heated at 80° C. for 20 h
  2. 2
    استخلاصThe solution is extracted repeatedly with dichloromethane
  3. 3
    غسيلThe combined organic extracts are washed with water and saturated sodium chloride solution
  4. 4
    تجفيفdried over sodium sulphate
  5. 5
    ترشيحfiltered
  6. 6
    أخرىevaporated under reduced pressure
  7. 7
    أخرىThe solid obtained
  8. 8
    غسيلis washed with a little tert-butyl methyl ether
  9. 9
    ترشيحfiltered off
  10. 10
    أخرىdried under reduced pressure

الإجراء التجريبي

28.5 g (228 mol) of 3-methoxypyridin-2(1H)-one are dissolved in 850 ml of dimethyl sulphoxide, and 31 g (273 mmol) of potassium tert-butoxide are added at RT. The suspension is stirred at RT for 30 min, and 35 g (228 mmol) of 1-fluoro-2-methyl-4-nitrobenzene are then added, and the reaction solution is heated at 80° C. for 20 h. The solution is then carefully diluted with 1 l of water and adjusted to pH 1-2 using 1N hydrochloric acid. The solution is extracted repeatedly with dichloromethane. The combined organic extracts are washed with water and saturated sodium chloride solution, dried over sodium sulphate, filtered and evaporated under reduced pressure. The solid obtained is washed with a little tert-butyl methyl ether, filtered off and dried under reduced pressure. This gives 42.8 g (72% of theory) of the desired compound.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08846934B2uspto-grants-2014_09