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Sodium Hydroxide → 4-Bromo-2-(1H-1,2,4-triazol-3-yl)aniline

HRID 2066406
ノート
印刷プレビュー

反応式

HRID 2066406 の反応式
[Br:1][C:2]1[CH:11]=[CH:10][C:9]2[NH:8]C(=O)[N:6]3[N:13]=[CH:14][N:15]=[C:5]3[C:4]=2[CH:3]=1.[OH-].[Na+]>C(O)CO>[Br:1][C:2]1[CH:11]=[CH:10][C:9]([NH2:8])=[C:4]([C:5]2[NH:6][N:13]=[CH:14][N:15]=2)[CH:3]=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

4

反応物 2

HCID 14798Sodium HydroxideHCID 1357668559-Bromo-[1,2,4]triazolo[1,5-c]quinazolin-5(6H)-one

生成物 1

HCID 620726444-Bromo-2-(1H-1,2,4-triazol-3-yl)aniline収率 87%

試薬・触媒・溶媒 1

HCID 174Ethylene Glycol溶媒

反応条件

温度
140 °C

実験手順

To a well stirred slurry of 9-bromo-6H-[1,2,4]triazolo[1,5-c]quinazolin-5-one (32.0 g, 171 mmol) in ethylene glycol (146 mL) which was heated at 100° C., was added aqueous NaOH (32%, 22.4 ml, 241 mmol). The slurry was heated at 140° C. for 17.5 h. The resulting solution was cooled to 27° C. and the product began to crystallize. Water (146 mL) and 1-octanol (1.73 mL) were added and the pH of the suspension was adjusted to 6.5 by the slow addition of glacial acetic acid (14 mL). The resulting slurry was stirred for 30 min, the solid was collected by filtration and washed with water and 2-propanol. Drying in vacuo afforded the title compound (25.2 g, 87%) as a light yellow solid. MS: m/e=239.0/241.1 [M+H+].

後処理

  1. temperatureThe resulting solution was cooled to 27° C.
  2. customto crystallize
  3. additionWater (146 mL) and 1-octanol (1.73 mL) were added
  4. additionthe pH of the suspension was adjusted to 6.5 by the slow addition of glacial acetic acid (14 mL)
  5. filtrationthe solid was collected by filtration
  6. washwashed with water and 2-propanol
  7. customDrying in vacuo

出典と根拠

ORDレコード
ord-b7af699befca4112acd43e08a64d7674
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08293730B2

反応ノート

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