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Hydrogen Bromide → 2-Bromo-5-phenyl-1,3,4-thiadiazole

HRID 747926
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HRID 747926 반응식
S(O)(O)(=O)=O.N[C:7]1[S:8][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:10][N:11]=1.[BrH:18].N([O-])=O.[Na+]>C(Cl)Cl.O>[Br:18][C:7]1[S:8][C:9]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[N:10][N:11]=1
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참가 물질

6

반응물 3

HCID 260Hydrogen BromideHCID 162130872-amino-5-phenyl-1,3,4-thiadiazole sulfate saltHCID 23668193Sodium Nitrite

생성물 1

HCID 131041172-Bromo-5-phenyl-1,3,4-thiadiazole수율 74%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매

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온도
5 °C

실험 절차

A mixture of 2-amino-5-phenyl-1,3,4-thiadiazole sulfate (Aldrich, 2.5 g, 9.08 mmol) and 48% aqueous HBr (10 mL) was cooled to 5° C. and a solution of NaNO2 (0.69 g, 9.99 mmol) H2O (10 mL) was added dropwise at a rate so the internal temperature is maintained at approximately 5° C. The mixture was stirred for 15 min after the addition, then CuBr (0.69 g, 4.8 mmol) was added portion-wise so as to maintain the temperature at approximately 5° C. After the addition was complete, the mixture was allowed to warm to ambient temperature and stirred for 16 h. The mixture was diluted with 20 mL CH2Cl2 and 10 mL H2O. The organic layer was separated and concentrated under reduced pressure to provide the title compound (1.63 g, 6.76 mmol, 74% yield). MS (DCl/NH3) m/z 241, 243 (M+H)+.

후처리

  1. temperatureis maintained at approximately 5° C
  2. additionafter the addition
  3. temperatureto maintain the temperature at approximately 5° C
  4. additionAfter the addition
  5. temperatureto warm to ambient temperature
  6. stirringstirred for 16 h
  7. customThe organic layer was separated
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3b15d66f1a9540cdb4d2a07549298b33
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07399765B2

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