تفاعل #167183

ord-5889963c010d4542a18235b144e16bd8

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONis slowly added in portions such that the temperature
  2. 2
    أخرىdoes not rise above 0° C
  3. 3
    workup.ADDITIONAfter completion of the addition
  4. 4
    workup.ADDITIONThe dark purple mixture is poured onto water (300 mL)
  5. 5
    استخلاصextracted twice with EA (300 mL)
  6. 6
    غسيلThe organic extracts are washed with sat. aq. NaHCO3, 0.5 N aq. HCl
  7. 7
    أخرىevaporated
  8. 8
    ترشيحfiltered off
  9. 9
    غسيلwashed with additional diethyl ether
  10. 10
    أخرىdried under high vacuum

الإجراء التجريبي

A solution of aniline (9.31 g, 100 mmol) and triethylamine (15.2 g, 150 mmol) in THE (150 mL) is cooled to −40° C. before chloroacetic acid chloride (11.3 g, 100 mmol) is slowly added in portions such that the temperature does not rise above 0° C. After completion of the addition, the brown suspension is stirred at rt for 1 h. The dark purple mixture is poured onto water (300 mL) and extracted twice with EA (300 mL). The organic extracts are washed with sat. aq. NaHCO3, 0.5 N aq. HCl, followed by water, and evaporated. The brown residue is suspended in diethyl ether, filtered off, washed with additional diethyl ether and dried under high vacuum to give 2-chloro-N-phenyl-acetamide. LC-MS: tR=0.75 min, [M+1]+=170, 1H NMR (CDCl3): δ 8.22 (s br, 1H), 7.56-7.51 (m, 2H), 7.40-7.24 (m, 2H), 7.20-7.14 (m, 1H), 4.20 (s, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE045174E1uspto-grants-2014_09