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Sodium Hydroxide → (E)-N-[(3-Fluorophenyl)methylidene]hydroxylamine

HRID 83200
ノート
印刷プレビュー

反応式

HRID 83200 の反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=O.Cl.[NH2:11][OH:12].[OH-].[Na+]>C(O)C.O>[F:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)/[CH:5]=[N:11]\[OH:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 14798Sodium HydroxideHCID 680093-FluorobenzaldehydeHCID 443297Hydroxyamine hydrochloride

生成物 1

HCID 5582750(E)-N-[(3-Fluorophenyl)methylidene]hydroxylamine収率 93.2%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒2 回
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

実験手順

To a suspension of 3-fluorobenzaldehyde (6.75 g, 54 mmol) and hydroxylamine hydrochloride (4.16 g, 60 mmol) in ethanol (4.3 mL) and water (13 mL) was added ice (25 g). Then a solution of sodium hydroxide (5.5 g, 138 mmol) in water (6.5 mL) was added dropwise within a 10 min period (temperature rises from −8° C. to +7° C.) whereupon most of the solid dissolves. After 30 min stirring at room temperature a white solid precipitated and the resulting mixture was then diluted with water and acidified with HCl (4 N). The white precipitate was then filtered off, washed with water and dried under high vacuum to afford the title compound (7.0 g, 93%) which was obtained as a white solid. MS m/e (EI): 139.1 [M].

後処理

  1. dissolutiondissolves
  2. customprecipitated
  3. additionthe resulting mixture was then diluted with water
  4. filtrationThe white precipitate was then filtered off
  5. washwashed with water
  6. customdried under high vacuum

出典と根拠

ORDレコード
ord-41b6cb3258f84ca38fcd74634933e5ab
出典データセット
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08846719B2

反応ノート

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