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Sulfuric Acid → HCID 53415966, 화합물

HRID 225669
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HRID 225669 반응식
[F:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1N.S(=O)(=O)(O)O.N([O-])=O.[Na+].[I-:20].[K+]>O>[F:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[I:20]
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참가 물질

6

반응물 4

HCID 1118Sulfuric AcidHCID 4875Potassium IodideHCID 23668193Sodium NitriteHCID 534170402-Fluoro-4,5-dimethylaniline

생성물 1

HCID 53415966HCID 53415966, 화합물수율 69%

시약·촉매·용매 1

HCID 962Water용매4회

실험 절차

To a stirred suspension of 50.8 mmol 2-fluoro-4,5-dimethyl-phenylamine-(commercial, CAS: 117832-17-4) in 70 ml water was added dropwise at 0° C. a solution of 5 ml concentrated sulfuric acid in 15 ml water. A solution of 66.0 mmol sodium nitrite in 15 ml water was then added dropwise and stirring continued at 0° C. for 60 min. A solution of 173 mmol potassium iodide in 50 ml water was then added dropwise over 30 min while maintaining the reaction temperature between 0 and 5° C. The reaction mixture was then warmed to room temperature and stirred for 3 h before being quenched with aqueous sodium thiosulphite solution and diluted with ethyl acetate. The phases were separated and the organic phase was washed with water and then dried over sodium sulfate and concentrated in vacuo to yield the title compound as a brown solid (69% yield). MS (m/e): 251 ([M+H]+, 100%).

후처리

  1. temperaturewhile maintaining the reaction temperature between 0 and 5° C
  2. stirringstirred for 3 h
  3. custombefore being quenched with aqueous sodium thiosulphite solution
  4. additiondiluted with ethyl acetate
  5. customThe phases were separated
  6. washthe organic phase was washed with water
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-3848bccb4675415e97fefa6b7cf83b93
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07557114B2

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