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Chloroform → 4-[2-(1H-Imidazol-1-yl)ethoxy]aniline

HRID 980146
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HRID 980146 반응식
[N+:1]([C:4]1[CH:17]=[CH:16][C:7]([O:8][CH2:9][CH2:10][N:11]2[CH:15]=[CH:14][N:13]=[CH:12]2)=[CH:6][CH:5]=1)([O-])=O.[OH-].[Na+].C(Cl)(Cl)Cl>Cl.[Fe]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([O:8][CH2:9][CH2:10][N:11]2[CH:15]=[CH:14][N:13]=[CH:12]2)=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 6212ChloroformHCID 14798Sodium HydroxideHCID 135691861-(2-(P-NO2Phenoxy)ethyl)imidazole

생성물 1

HCID 135692034-[2-(1H-Imidazol-1-yl)ethoxy]aniline수율 69.8%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 313Hydrochloric Acid용매

실험 절차

Iron powder (6.0 g) was added in portions to a warm solution of 1-[2-(4-nitrophenoxy)ethyl]imidazole (3.7 g) in 5N hydrochloric acid (60 ml). After 20 minutes the solution was cooled, made basic with dilute sodium hydroxide solution and the mixture was shaken with chloroform and filtered. The chloroform layer of the filtrate was separated, dried (Na2SO4) and evaporated to give a solid which was crystallised from ethyl acetate/petrol to give 1-[2-(4-aminophenoxy)ethyl]imidazole (2.25 g) m.p. 91°-92° C. Found: C, 64.35; H, 6.40; N, 20.61. C11H13N3O requires: C, 65.01; H, 6.45; N, 20.68%.

후처리

  1. temperatureAfter 20 minutes the solution was cooled
  2. filtrationfiltered
  3. customThe chloroform layer of the filtrate was separated
  4. dry with materialdried (Na2SO4)
  5. customevaporated
  6. customto give a solid which
  7. customwas crystallised from ethyl acetate/petrol

출처 및 근거

ORD 기록
ord-dcdeb42254ea4685995ca6716bd58609
출처 데이터셋
uspto-grants-1987_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04636500

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