Ammonia → N-(2,4,6-tribromophenyl)glycinamide

HRID 1995764

반응식

HRID 1995764 반응식
[Br:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([Br:9])[C:3]=1[NH:10]CC(OCC)=O.[NH3:17].[CH2:18]([OH:20])[CH3:19]>>[Br:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([Br:9])[C:3]=1[NH:10][C:18](=[O:20])[CH2:19][NH2:17]

참가 물질

4

반응물 3

HCID 222AmmoniaHCID 702EthanolHCID 12659467ethyl N-(2,4,6-tribromophenyl)glycinate

생성물 1

HCID 28992175N-(2,4,6-tribromophenyl)glycinamide

실험 절차

IV (7.5 g, 0.018 mole) and absolute ethanol (300 ml) were placed in a flask and warmed slightly to dissolve all of the crystals. Then the solution was saturated with anhydrous ammonia while the flask was cooled in ice water. White needles separated after the clear solution stood at room temperature for 3 days. The mixture was cooled in ice water, and the crystals were filtered and washed with a small amount of cold ethanol. A second crop of crystals, 1.1 g, was obtained by evaporating the filtrate to a volume of 35 ml and cooling in ice water. The total yield was 6.1 g (89%), mp 185°-185.5° C. Anal. calcd. for C8H7Br3N2O: C, 24.84; H, 1.82; Br, 61.96; N, 7.24. Found: C, 24.83; H, 1.87; Br, 61.82; N, 7.26.

후처리

  1. temperaturewarmed slightly
  2. dissolutionto dissolve all of the crystals
  3. customWhite needles separated after the clear solution
  4. temperatureThe mixture was cooled in ice water
  5. filtrationthe crystals were filtered
  6. washwashed with a small amount of cold ethanol
  7. customA second crop of crystals, 1.1 g, was obtained
  8. customby evaporating the filtrate to a volume of 35 ml
  9. temperaturecooling in ice water

출처 및 근거

ORD 기록
ord-48af771a32e749edbe69946100bc49d3
출처 데이터셋
uspto-grants-1983_09
특허 번호
US04405806

연결된 노트

불러오는 중…