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Benzaldehyde → 2-(Dimethoxymethyl)-3-phenylacrylonitrile

HRID 496819
ノート
印刷プレビュー

反応式

HRID 496819 の反応式
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][O:10][CH:11]([O:15][CH3:16])[CH2:12][C:13]#[N:14].C[O-].[Na+]>CO>[CH3:9][O:10][CH:11]([O:15][CH3:16])[C:12](=[CH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:13]#[N:14]
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 3

HCID 240BenzaldehydeHCID 937313,3-DimethoxypropiononitrileHCID 10942334Sodium Methoxide

生成物 1

HCID 538099012-(Dimethoxymethyl)-3-phenylacrylonitrile収率 68%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Benzaldehyde (79.5 g, 0.75 mol) and 3,3-dimethoxypropionitrile (115.1 g, 1.0 mol) were mixed together and added to a solution of sodium methoxide (54.0 g, 1.0 mol) in methanol (400 mL) over a period of 15 minutes. The mixture was stirred at room temperature overnight. Most of the methanol was evaporated in vacuo and the residue was partitioned between ethyl acetate (500 mL) and water (450 mL). The organic layer was separated, washed with brine (400 mL), dried (MgSO4) and the solvent evaporated in vacuo. The residual oil was distilled to give 103 g (68%) of the product as a colorless oil, bp 125-130° C. (2 mm Hg).

後処理

  1. customMost of the methanol was evaporated in vacuo
  2. customthe residue was partitioned between ethyl acetate (500 mL) and water (450 mL)
  3. customThe organic layer was separated
  4. washwashed with brine (400 mL)
  5. dry with materialdried (MgSO4)
  6. customthe solvent evaporated in vacuo
  7. distillationThe residual oil was distilled

出典と根拠

ORDレコード
ord-2dbbaa9df03f4353865da47aa9bc6ae9
出典データセット
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06946554B2

反応ノート

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