Water → 3,3,3-Trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)

HRID 48483

反応式

HRID 48483 の反応式
C([O-])(=O)C.[Na+].O.Br[CH:8](Br)[C:9]([C:11]([F:14])([F:13])[F:12])=[O:10].[F:16][C:17]1[CH:22]=[C:21]([Cl:23])[C:20]([O:24][CH:25]([CH3:27])[CH3:26])=[CH:19][C:18]=1[NH:28][NH2:29]>C(OCC)C>[Cl:23][C:21]1[C:20]([O:24][CH:25]([CH3:26])[CH3:27])=[CH:19][C:18]([NH:28][N:29]=[CH:8][C:9](=[O:10])[C:11]([F:14])([F:13])[F:12])=[C:17]([F:16])[CH:22]=1

参加物

6

反応物 4

HCID 962WaterHCID 185080(4-Chloro-2-fluoro-5-propan-2-yloxyphenyl)hydrazineHCID 517045Sodium AcetateHCID 5505231,1-Dibromo-3,3,3-trifluoroacetone

生成物 1

HCID 691414303,3,3-Trifluoro-2-oxopropanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To a mixed solution of 5.3 g (53.5 mmol) of sodium acetate and about 100 ml of water was added under ice cooling 6.6 g (24.3 mmol) of 1,1-dibromo-3,3,3-trifluoroacetone, and the reaction was allowed to proceed at 70° C. for 20 minutes. Then, the reaction mixture was cooled to room temperature, to which a solution of 5.8 g (21.5 mmol) of 2-fluoro-4-chloro-5-isopropoxyphenylhydrazine dissolved in about 20 ml of diethyl ether was added, and the reaction mixture was stirred at room temperature for 1 hour. The ether layer was separated, washed once with 10 ml of saturated sodium chloride solution, and dried with magnesium sulfate. The diethyl ether was distilled out, which afforded 6.5 g (20.0 mmol) of 3,3,3-trifluoro-2-oxo-propanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone).

後処理

  1. additionwas added
  2. customThe ether layer was separated
  3. washwashed once with 10 ml of saturated sodium chloride solution
  4. dry with materialdried with magnesium sulfate
  5. distillationThe diethyl ether was distilled out

出典と根拠

ORDレコード
ord-285974394a6940eb86913218fa000983
出典データセット
uspto-grants-2004_03
特許番号
US06703503B2

関連ノート

読み込み中…