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3-Bromo-1,1,1-trifluoro-2-propanone → 2-Propanone,3-bromo-1,1,1-trifluoro-, oxime

HRID 18499
ノート
印刷プレビュー

反応式

HRID 18499 の反応式
[Br:1][CH2:2][C:3](=O)[C:4]([F:7])([F:6])[F:5].Cl.[NH2:10][OH:11]>C(Cl)(Cl)Cl.O>[Br:1][CH2:2][C:3](=[N:10][OH:11])[C:4]([F:7])([F:6])[F:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 790083-Bromo-1,1,1-trifluoro-2-propanoneHCID 443297Hydroxyamine hydrochloride

生成物 1

HCID 27822732-Propanone,3-bromo-1,1,1-trifluoro-, oxime収率 55.7%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6212Chloroform溶媒

実験手順

To a solution of 10.5 mL (102.3 mmol) of 1-bromo-3,3,3-trifluoropropan-2-one in 100 mL of chloroform (passed through a pad of basic Al2O3) was added a solution of 10.4 g (149.7 mmol) of hydroxylamine hydrochloride in 20 mL of water and the mixture was warmed at reflux. After 24 hours, the mixture was cooled and the organic phase was separated. The aqueous layer was extracted with three 30 mL portions of methylene chloride. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 11.5 g (55.7%) of 3-bromo-1,1,1-trifluoropropan-2-one oxime as a mixture (3:2) of geometric isomers.

後処理

  1. temperaturethe mixture was warmed
  2. temperatureat reflux
  3. temperaturethe mixture was cooled
  4. customthe organic phase was separated
  5. extractionThe aqueous layer was extracted with three 30 mL portions of methylene chloride
  6. dry with materialThe combined organic layers were dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-b02136aa83d1400b8c455afe45498dcf
出典データセット
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07741361B2

反応ノート

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