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Ammonium Chloride → 4-Chloro-5-iodobenzene-1,2-diamine

HRID 340764
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HRID 340764 반응식
[Cl:1][C:2]1[C:3]([I:12])=[CH:4][C:5]([N+:9]([O-])=O)=[C:6]([CH:8]=1)[NH2:7].[NH4+].[Cl-]>CCO.O.[Fe]>[Cl:1][C:2]1[CH:8]=[C:6]([NH2:7])[C:5]([NH2:9])=[CH:4][C:3]=1[I:12]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 25517Ammonium Chloride2회HCID 223175485-Chloro-4-iodo-2-nitroaniline

생성물 1

HCID 574814674-Chloro-5-iodobenzene-1,2-diamine

시약·촉매·용매 3

HCID 23925Iron촉매2회HCID 702Ethanol용매HCID 962Water용매

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
50 °C

실험 절차

To a suspension of 5-chloro-4-iodo-2-nitroaniline (36.5 g, 122 mmol) in EtOH (800 mL) and water (150 mL) was added iron powder (38 g, 673 mmol) and NH4Cl (16 g, 306 mmol). The mixture was heated under nitrogen at 50° C. overnight. Additional iron powder (38 g, 673 mmol) and NH4Cl (16 g, 306 mmol) were added and heating was continued for 45 h. The reaction mixture was cooled, filtered and concentrated. The resulting residue was re-dissolved in ethyl acetate and washed with sodium bicarbonate solution. The organic phase was concentrated to afford the desired product as a gray solid, which was used in the next step without further purification.

후처리

  1. temperatureheating
  2. temperatureThe reaction mixture was cooled
  3. filtrationfiltered
  4. concentrationconcentrated
  5. dissolutionThe resulting residue was re-dissolved in ethyl acetate
  6. washwashed with sodium bicarbonate solution
  7. concentrationThe organic phase was concentrated

출처 및 근거

ORD 기록
ord-ca4ef106e17047ae8e06ce1b93002fad
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895596B2

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