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Water → Benzaldehyde, 4-(trifluoromethyl)-, oxime

HRID 843359
ノート
印刷プレビュー

反応式

HRID 843359 の反応式
[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=O)=[CH:5][CH:4]=1.Cl.[NH2:14][OH:15].O.[OH-].[Na+]>C(O)C.CCOCC>[F:1][C:2]([F:12])([F:11])[C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[N:14][OH:15])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 679964-(Trifluoromethyl)benzaldehydeHCID 443297Hydroxyamine hydrochloride

生成物 1

HCID 3056297Benzaldehyde, 4-(trifluoromethyl)-, oxime収率 95.5%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒
このページの内容参加物実験手順後処理出典と根拠反応ノート
HCID 3283
Diethyl Ether
溶媒

実験手順

The first step of the process of the present invention was conducted as follows. At first, 8.79 g (50.5 mmol) of 4-trifluoromethylbenzaldehyde and 3.83 g (55.1 mmol) of hydroxylamine hydrochloride were dissolved in 12.5 ml of ethanol and 34 ml of water followed by the addition of 2.5 g of sodium hydroxide and stirring for 1 hour at room temperature. After adding ether and washing with dilute hydrochloric acid, the reaction liquid was further washed with saturated brine followed by drying with mirabilite and concentrating to obtain 9.25 g (48.2 mmol) of 4-trifluoromethylbenzaldehyde oxime (yield: 95.5%).

後処理

  1. washwashing with dilute hydrochloric acid
  2. customthe reaction liquid
  3. washwas further washed with saturated brine
  4. dry with materialby drying with mirabilite
  5. concentrationconcentrating

出典と根拠

ORDレコード
ord-155f64241f6e4c2ebd5c431fcaf9a6c9
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06376712B2

反応ノート

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