تفاعل #2446147

ord-3ca8dc5169c74aba8ef26f2003afa8ee

معادلة التفاعل

[Cl-].[NH4+]
ammonium chloride
O=C(CCl)Nc1ccc(Br)cc1[N+](=O)[O-]
N-(4-bromo-2-nitrophenyl)-2-chloroacetamide
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
CC(=O)O
acetic acid
Nc1cc(Br)ccc1NC(=O)CCl
N-(2-amino-4-bromophenyl)-2-chloroacetamide
المردود 43.3%

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGAfter stirring for 15 min
  2. 2
    ترشيحThe remaining solids were filtered
  3. 3
    غسيلwashed with water and ethyl acetate
  4. 4
    استخلاصExtraction of the water layer with ethyl acetate
  5. 5
    غسيلwashing of the combined organic layers with brine
  6. 6
    تجفيفdrying over MgSO4
  7. 7
    أخرىremoving the solvent
  8. 8
    أخرىunder reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1)

الإجراء التجريبي

Ferrous powder (19.8 g, 354 mmol), ammonium chloride (1.1 g, 19.7 mmol) and acetic acid (4.9 ml, 86.5 mmol) were suspended in 300 ml water and stirred at 50° C. for 15 min. To this mixture, a solution of N-(4-bromo-2-nitrophenyl)-2-chloroacetamide (11.5 g, 39.3 mmol) in 100 ml DMF was added quickly. After stirring for 15 min, the mixture was basified to pH 9 with aqueous sodium carbonate solution. The remaining solids were filtered and washed with water and ethyl acetate. Extraction of the water layer with ethyl acetate, washing of the combined organic layers with brine, drying over MgSO4, removing the solvent under reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1) yielded N-(2-amino-4-bromophenyl)-2-chloroacetamide (4.5 g, 17.0 mmol, 43%) as an off-white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685960B2uspto-grants-2014_04