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Sodium Hydroxide → 3-(4-(3-(Trifluoromethyl)phenoxy)phenyl)acrylonitrile

HRID 705843
ノート
印刷プレビュー

反応式

HRID 705843 の反応式
[Br-].[C:2]([CH2:4][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)#[N:3].[OH-].[Na+].[F:26][C:27]([F:44])([F:43])[C:28]1[CH:29]=[C:30]([CH:40]=[CH:41][CH:42]=1)[O:31][C:32]1[CH:39]=[CH:38][C:35]([CH:36]=O)=[CH:34][CH:33]=1>O.C(Cl)Cl>[F:26][C:27]([F:44])([F:43])[C:28]1[CH:29]=[C:30]([CH:40]=[CH:41][CH:42]=1)[O:31][C:32]1[CH:39]=[CH:38][C:35]([CH:36]=[CH:4][C:2]#[N:3])=[CH:34][CH:33]=1
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 11811037(Cyanomethyl)triphenylphosphonium bromideHCID 121487884-(3-(Trifluoromethyl)phenoxy)benzaldehyde

生成物 1

HCID 677761303-(4-(3-(Trifluoromethyl)phenoxy)phenyl)acrylonitrile収率 92%

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回
HCID 6344
Dichloromethane
溶媒
2 回

実験手順

To a solution of (cyanomethyl)triphenylphosphonium bromide (8.61 g, 22.54 mmol) and NaOH (1.127 g, 28.2 mmol) in water (24 mL) and DCM (12 mL) was added 4-(3-(trifluoromethyl)phenoxy)benzaldehyde (5 g, 18.78 mmol) at 0° C. The mixture was stirred at room temperature for 4 h. DCM (50 mL) and water (50 mL) was added to the mixture, the organic phase was washed with water (50 mL), brine (50 mL), dried over anhydrous sodium sulfate and concentrated. Purification via flash chromatography afforded the title compound (5.07 g, 17.26 mmol, 92% yield) as pale yellow oil (slowly solidify to white solid). LCMS: rt=1.67 min, [M+H+]=290

後処理

  1. washthe organic phase was washed with water (50 mL), brine (50 mL)
  2. dry with materialdried over anhydrous sodium sulfate
  3. concentrationconcentrated
  4. customPurification via flash chromatography

出典と根拠

ORDレコード
ord-ce85193388d447e2a94938153a889161
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09174968B2

反応ノート

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