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Sodium Cyanide → 2,4-Dibromo-6-cyanomethylanisole

HRID 1155976
ノート
印刷プレビュー

反応式

HRID 1155976 の反応式
[Br:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([CH2:9]Br)[C:3]=1[O:11][CH3:12].[C-:13]#[N:14].[Na+]>C(O)C.O>[Br:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[C:4]([CH2:9][C:13]#[N:14])[C:3]=1[O:11][CH3:12]
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 8929Sodium CyanideHCID 205361872,4-Dibromo-6-bromomethylanisole

生成物 1

HCID 205361852,4-Dibromo-6-cyanomethylanisole

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

A solution of the product of stage (c) (183 g) in ethanol (150 ml) was heated to reflux. A solution of sodium cyanide (25 g) in hot water (50 ml) was added which maintained gentle refluxing. The mixture was then stirred for 5 minutes, poured into ice water, and the product was filtered off, taken up in dichloromethane, washed with water, dried over magnesium sulphate and filtered. The solvent was removed to give a brown oil which slowly crystallised. Recrystallisation from petroleum ether gave the title product as colourless needles, mp 87°-88° C.

後処理

  1. temperaturemaintained gentle refluxing
  2. filtrationthe product was filtered off
  3. washwashed with water
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customThe solvent was removed
  7. customto give a brown oil which
  8. customslowly crystallised
  9. customRecrystallisation from petroleum ether

出典と根拠

ORDレコード
ord-696e7177b0634e3584ddd9965c0848bf
出典データセット
uspto-grants-1982_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04333759

反応ノート

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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