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Hydrogen Bromide → HCID 66980994, 화합물

HRID 2279247
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HRID 2279247 반응식
N[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]([F:13])([F:12])[F:11])[C:3]=1[CH3:14].N([O-])=O.[Na+].[BrH:19]>O>[Br:19][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([C:10]([F:13])([F:12])[F:11])[C:3]=1[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 260Hydrogen Bromide2회HCID 218752104-Amino-3-methyl-2-(trifluoromethyl)benzonitrileHCID 23668193Sodium Nitrite

생성물 1

HCID 66980994HCID 66980994, 화합물수율 60%

시약·촉매·용매 1

HCID 962Water용매3회

실험 절차

To a solution of 4-amino-3-methyl-2-(trifluoromethyl)benzonitrile (3e) (0.8 g, 4.0 mmol) in water (2 mL), cooled to 0° C., 48% aqueous HBr (10 mL, 18.5 mmol) was added followed by NaNO2 (0.33 g, 4.8 mmol) taken in water (2 mL) and stirred for 10 min. To the reaction mixture a solution of CuBr (2.7 g, 18.8 mmol) in HBr (10 mL) was added at 0° C. and slowly warmed to room temperature and then heated to 50° C. for 1 h. The reaction mixture was brought to room temperature, diluted with water (50 mL) and extracted with EtOAc (3×20 mL). The combined organic extracts were washed with water (2×20 mL), dried over Na2SO4 and concentrated under reduced pressure to give the crude compound which was purified by column chromatography to provide the bromo 3f (0.6 g, 60%) as a tan colored solid.

후처리

  1. temperatureheated to 50° C. for 1 h
  2. customwas brought to room temperature
  3. extractionextracted with EtOAc (3×20 mL)
  4. washThe combined organic extracts were washed with water (2×20 mL)
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated under reduced pressure
  7. customto give the crude compound which
  8. customwas purified by column chromatography

출처 및 근거

ORD 기록
ord-15b85f9ddce444fcb5183ec4bc7dadf4
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133182B2

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