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Ammonium Chloride → HCID 22033543, 화합물

HRID 325028
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HRID 325028 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][CH2:11][CH2:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]#[N:20])=[CH:15][CH:14]=2)[CH:5]=1)([O-])=O.[NH4+].[Cl-]>CCO.O.[Fe]>[NH2:1][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][CH2:11][CH2:12][C:13]2[CH:14]=[CH:15][C:16]([C:19]#[N:20])=[CH:17][CH:18]=2)[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 25517Ammonium ChlorideHCID 22033514Nitro-3-[2-(4-cyanophenyl)ethoxy]benzene

생성물 1

HCID 22033543HCID 22033543, 화합물수율 85%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 702Ethanol용매HCID 962Water용매

실험 절차

Nitro-3-[2-(4-cyanophenyl)ethoxy]benzene (3.0 g; 11.2 mmol; from step (i) above) and NH4Cl (2.9 g; 55 mmol) were dissolved in a mixture of EtOH (40 mL) and H2O (10 mL) and heated to reflux. Iron powder (3.0 g; 55 mmol) was added and heating was continued for 1 hour. The mixture was filtered, concentrated in vacuo and partitioned between water and CH2Cl2. After separation, the aqueous phase was extracted with CH2Cl2. The combined organic phases were dried (MgSO4) and the solvent was evaporated. Purification by flash chromatography (SiO2; toluene:EtOAc (9:1)) afforded 2.26 g (85%) of the sub-title compound.

후처리

  1. temperatureheated to reflux
  2. temperatureheating
  3. filtrationThe mixture was filtered
  4. concentrationconcentrated in vacuo
  5. custompartitioned between water and CH2Cl2
  6. customAfter separation
  7. extractionthe aqueous phase was extracted with CH2Cl2
  8. dry with materialThe combined organic phases were dried (MgSO4)
  9. customthe solvent was evaporated
  10. customPurification by flash chromatography (SiO2; toluene:EtOAc (9:1))

출처 및 근거

ORD 기록
ord-8ef99bd1e03243c586593e9f31e39f13
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06221898B1

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