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Phosphorus tribromide → 1-(Bromomethyl)-2-(trifluoromethyl)benzene

HRID 326701
ノート
印刷プレビュー

反応式

HRID 326701 の反応式
P(Br)(Br)[Br:2].[F:5][C:6]([F:16])([F:15])[C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH2:9]O>C1(C)C=CC=CC=1>[F:5][C:6]([F:16])([F:15])[C:7]1[CH:14]=[CH:13][CH:12]=[CH:11][C:8]=1[CH2:9][Br:2]
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 24614Phosphorus tribromideHCID 676662-(Trifluoromethyl)benzylic alcohol

生成物 1

HCID 1230571-(Bromomethyl)-2-(trifluoromethyl)benzene

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

A solution of 30 ml of phosphorus tribromide in 60 ml of absolute toluene was added dropwise at 20°-30° C. to a solution of 14 g of o-trifluoromethylbenzyl alcohol in 80 ml of absolute toluene. Subsequently, the reaction mixture was stirred at room temperature for 2 hours, the toluene was distilled under reduced pressure, the residue was dissolved in methylene chloride, treated with water and the mixture was adjusted to pH 8.0 with potassium hydrogen carbonate. The aqueous phase was extracted three times with CH2Cl2 and the organic phases were washed twice with water and once with saturated NaCl solution, dried over Na2SO4 and evaporated under reduced pressure. o-Trifluoromethylbenzyl bromide was obtained as the residue.

後処理

  1. distillationthe toluene was distilled under reduced pressure
  2. dissolutionthe residue was dissolved in methylene chloride
  3. additiontreated with water
  4. extractionThe aqueous phase was extracted three times with CH2Cl2
  5. washthe organic phases were washed twice with water and once with saturated NaCl solution
  6. dry with materialdried over Na2SO4
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-0569fc5a788c47769d676e97dce0c4c1
出典データセット
uspto-grants-1993_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05270313

反応ノート

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