Chloral Hydrate → HCID 87327711、化合物
反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH:6]=[C:7]([F:9])[CH:8]=1)[NH2:5].Cl[C:11](Cl)(Cl)[CH:12]([OH:14])O.[O-]S([O-])(=O)=O.[Na+].[Na+].[Cl-].[OH:25][NH3+:26]>Cl.O>[Br:1][C:2]1[CH:3]=[C:4]([NH:5][C:12](=[O:14])/[CH:11]=[N:26]/[OH:25])[CH:6]=[C:7]([F:9])[CH:8]=1参加物
7
実験手順
A mixture of 3-bromo-5-fluoroaniline (4.0 g, 21.1 mmol, 1.0 equiv) in conc. HCl (10 mL) and water (100 mL) was heated until it became a clear solution. 2,2,2-trichloroethane-1,1-diol (3.83 g, 23.2 mmol, 1.1 equiv) and Na2SO4 (22.5 g, 158.5 mmol, 7.3 equiv.) was pre-warmed to 50° C. and added to the mixture. To the stirred mixture was then added an aqueous solution of hydroxylammonium chloride (4.39 g, 63.2 mmol, 3.0 equiv) dropwise. The resulting mixture was refluxed for 1 h. After it was cooled to room temperature, the precipitate was filtered and washed with excess water, dried under vacuum to provide 6.13 g of crude product, which was used into the next step without further purification. MS (ESI): 259, 261 (MH+).
後処理
- temperaturewas heated until it
- additionadded to the mixture
- temperatureThe resulting mixture was refluxed for 1 h
- filtrationthe precipitate was filtered
- washwashed with excess water
- customdried under vacuum
出典と根拠
- ORDレコード
- ord-e38aa9d880284845852574f43b91defb
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08772301B2
反応ノート
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