تفاعل #417965

ord-904dd1e5c9634532a7bdbe92ef1dfa80

معادلة التفاعل

CC(=O)OC(C)=O
Acetic anhydride
Cc1ccc(N)cc1O
5-amino-2-methyl phenol
CCOc1cccc(Br)c1
3-bromophenetole
O=C([O-])[O-].[Cs+].[Cs+]
Cs2CO3
CC(=O)Nc1ccc(C)c(OCCOc2ccccc2)c1
product 18a
CC(=O)Nc1ccc(C)c(OCCOc2ccccc2)c1
N-[4-methyl-3-(2-phenoxy-ethoxy)-phenyl]-acetamide

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةthe reaction was refluxed for 5 mins
  2. 2
    ترشيحIt was filtered off
  3. 3
    غسيلwashed with water (4 mL)
  4. 4
    أخرىdried
  5. 5
    أخرىto obtain the product along with the trace amount of O-acylated product
  6. 6
    استخلاصextracted with ethyl acetate (3×20 mL)
  7. 7
    تجفيفThe combined extracts were dried over sodium sulfate
  8. 8
    أخرىrecrystallized from toluene

الإجراء التجريبي

Acetic anhydride (1.25 mL, 12.2 mmol) was added to a solution of 5-amino-2-methyl phenol (1.0 g, 8.1 mmol) in acetic acid (6 mL), and the reaction was refluxed for 5 mins. Then the reaction mixture was cooled to room temperature and the product was solidified. It was filtered off and washed with water (4 mL) and dried to obtain the product along with the trace amount of O-acylated product. The mixture, to which was added 3-bromophenetole (1.33 g, 6.6 mmol) and Cs2CO3 (2.927 g, 9.0 mmol) in DMF (10 mL), was stirred overnight at 50° C. The reaction mixture was then diluted with water (10 mL) and extracted with ethyl acetate (3×20 mL). The combined extracts were dried over sodium sulfate and recrystallized from toluene to obtain the pure product 18a in 65% (yield over two steps) as an off-white solid.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08877752B2uspto-grants-2014_11