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Sodium Cyanide → 2-(2,6-Bis(trifluoromethyl)phenyl)acetonitrile

HRID 254477
ノート
印刷プレビュー

反応式

HRID 254477 の反応式
Br[CH2:2][C:3]1[C:8]([C:9]([F:12])([F:11])[F:10])=[CH:7][CH:6]=[CH:5][C:4]=1[C:13]([F:16])([F:15])[F:14].[C-:17]#[N:18].[Na+]>CCO.O>[F:14][C:13]([F:16])([F:15])[C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([C:9]([F:12])([F:11])[F:10])[C:3]=1[CH2:2][C:17]#[N:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 8929Sodium CyanideHCID 118513632,6-Bis(trifluoromethyl)benzyl bromide

生成物 1

HCID 589518382-(2,6-Bis(trifluoromethyl)phenyl)acetonitrile

試薬・触媒・溶媒 1

HCID 19096565Water ethanol溶媒

実験手順

A solution of 0.73 g (2.4 mmol) 2-bromomethyl-1,3-bis-trifluoromethyl-benzene and 0.183 g (3.7 mmol) sodium cyanide in 10 ml EtOH/H2O 6:1 (v/v) was hated to reflux for 3h. Then the reaction mixture was evaporated, the residue taken up in water and extracted with tert-butyl methyl ether. The combined extracts were washed with saturated aqueous NaHCO3 solution and brine, dried over Na2SO4 and evaporated. Purification by flash chromatography on silica gel with a gradient of 95:5 to 70:30% heptane/ethyl acetate provided (2,6-bis-trifluoromethyl-phenyl)-acetonitrile as colourless crystalline product of m.p. 84.5-86° C.: MS (EI): 253.0 (M.+ ), 234.1 ((M-F) .+), 233.1 ((M-HF)+.), 184.0 (((M-CF3)+.), 100%).

後処理

  1. temperatureto reflux for 3h
  2. customThen the reaction mixture was evaporated
  3. extractionextracted with tert-butyl methyl ether
  4. washThe combined extracts were washed with saturated aqueous NaHCO3 solution and brine
  5. dry with materialdried over Na2SO4
  6. customevaporated
  7. customPurification by flash chromatography on silica gel with a gradient of 95:5 to 70

出典と根拠

ORDレコード
ord-de33135fe59443bcb0ff58fff42f61a4
出典データセット
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07875645B2

反応ノート

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