Phosphine tribromide → 4'-(Bromomethyl)-2'-nitrobiphenyl-2-carbonitrile

HRID 1412590ノート

反応式

HRID 1412590 の反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:10]([C:15]#[N:16])=[CH:11][CH:12]=[CH:13][CH:14]=2)=[C:5]([N+:17]([O-:19])=[O:18])[CH:4]=1.[Br-:20].[Br-].[Br-].P>C1(C)C=CC=CC=1>[Br:20][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:10]([C:15]#[N:16])=[CH:11][CH:12]=[CH:13][CH:14]=2)=[C:5]([N+:17]([O-:19])=[O:18])[CH:4]=1

参加物

4

反応物 2

HCID 21862892Phosphine tribromideHCID 670092004'-(Hydroxymethyl)-2'-nitrobiphenyl-2-carbonitrile

生成物 1

HCID 670096674'-(Bromomethyl)-2'-nitrobiphenyl-2-carbonitrile

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

To a solution (15 mL) of 4′-(hydroxymethyl)-2′-nitrobiphenyl-2-carbonitrile (3.62 g) in toluene was added phosphine tribromide (4.63 g) at room temperature, and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated, and the residue was dissolved in ethyl acetate. The obtained ethyl acetate solution was washed with saturated aqueous sodium hydrogen carbonate and then with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography to give 4′-(bromomethyl)-2′-nitrobiphenyl-2-carbonitrile as a pale-yellow oil.

後処理

  1. concentrationThe reaction mixture was concentrated
  2. dissolutionthe residue was dissolved in ethyl acetate
  3. washThe obtained ethyl acetate solution was washed with saturated aqueous sodium hydrogen carbonate
  4. dry with materialwith saturated brine, and dried over anhydrous magnesium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. customthe residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-d0988174a2324cfda2802c779e001a5d
出典データセット
uspto-grants-2014_12
特許番号
US08921379B2

反応ノート

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