تفاعل #527720

ord-1d535b203d78433f9de20e65f2021495

معادلة التفاعل

CI
Methyl iodide
CI
Methyl iodide
Cc1cc(O)ccc1Cl
4-chloro-3-methylphenol
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C1CCC(=O)N1Br
N-bromosuccinimide
O=C(OOC(=O)c1ccccc1)c1ccccc1
benzoyl peroxide
COc1ccc(Cl)c(CBr)c1
2-chloro-5-methoxy benzyl bromide

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture stirred for a further hour
  2. 2
    أخرىSolvent was removed by evaporation
  3. 3
    أخرىthe residue partitioned between water and ethyl acetate
  4. 4
    أخرىThe organic layer yielded an oil which
  5. 5
    درجة الحرارةwas heated
  6. 6
    درجة الحرارةThe mixture was cooled
  7. 7
    ترشيحfiltered
  8. 8
    تركيزthe filtrate concentrated
  9. 9
    أخرىto give a residue which
  10. 10
    workup.DISTILLATIONwas distilled under high vacuum
  11. 11
    أخرىThe fractions collected between 88° and 94° C./0.4 mbar
  12. 12
    أخرىwere recrystallised from petroleum ether (b.p. 60°-80° C.)

الإجراء التجريبي

Methyl iodide (110 g was added dropwise to a stirred solution of 4-chloro-3-methylphenol (100 g) and potassium carbonate (194 g) in acetone (500 ml). The mixture was stirred for 1.5 hours. Methyl iodide (142 g) was added and the mixture stirred for a further hour. Solvent was removed by evaporation and the residue partitioned between water and ethyl acetate. The organic layer yielded an oil which was heated under reflux for 2 hours with N-bromosuccinimide (119 g) and benzoyl peroxide (1 g) in carbon tetrachloride (250 ml). The mixture was cooled, filtered and the filtrate concentrated to give a residue which was distilled under high vacuum. The fractions collected between 88° and 94° C./0.4 mbar were recrystallised from petroleum ether (b.p. 60°-80° C.) to give 2-chloro-5-methoxy benzyl bromide, m.p. 51°-52° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05519034uspto-grants-1996_05