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

HRID 253187
ノート
印刷プレビュー

反応式

HRID 253187 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒

反応条件

温度
5 °C

実験手順

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)+.

後処理

  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

出典と根拠

ORDレコード
ord-1742f78049334d6885a6f18a49f66fd4
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07872010B2

反応ノート

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