تفاعل #78290

ord-838b54af43ff4a799efbc77e83ff702c

معادلة التفاعل

Oc1ccccc1
phenol
O=[N+]([O-])c1ccc(Cl)c(O)c1
2-chloro-5-nitrophenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CC(C)=CCBr
4-bromo-2-methyl-2-butene
CC(C)=CCBr
prenyl bromide
CC(C)=CCOc1cc([N+](=O)[O-])ccc1Cl
1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for 2 hours
  2. 2
    أخرىThe solvent was then removed from the reaction mixture
  3. 3
    workup.ADDITIONThe residue of the reaction mixture was then treated with water
  4. 4
    استخلاصextracted into diethyl ether
  5. 5
    غسيلThe extract was washed with 2N sodium hydroxide and water
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    ترشيحfiltered
  8. 8
    أخرىevaporated
  9. 9
    أخرىto leave a brown solid which
  10. 10
    أخرىwas recrystallised from ethyl acetate/isopropyl alcohol

الإجراء التجريبي

A reaction mixture of 2-chloro-5-nitrophenol (50.6 g), anhydrous potassium carbonate (44.5 g), tetrabutylammonium bromide (4.7 g) and 4-bromo-2-methyl-2-butene (53.3 g, 90%) in methyl ethyl ketone (263 mL) was stirred at ambient temperature overnight. TLC of the reaction mixture showed traces of phenol remaining. Additional prenyl bromide (1 mL) was then added to the reaction mixture and stirred for 2 hours. The solvent was then removed from the reaction mixture. The residue of the reaction mixture was then treated with water and extracted into diethyl ether. The extract was washed with 2N sodium hydroxide and water, dried (MgSO4), filtered, and evaporated, to leave a brown solid which was recrystallised from ethyl acetate/isopropyl alcohol to give 1-chloro-2-(3-methyl-2-butenyloxy)-4-nitrobenzene, 49.5 g, a beige solid, a single spot on TLC (ethyl acetate:hexane, 20:80).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06710077B1uspto-grants-2004_03