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Phosphorus tribromide → 1-(Bromomethyl)-4-iodo-2-(trifluoromethyl)benzene

HRID 1946394
ノート
印刷プレビュー

反応式

HRID 1946394 の反応式
[I:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8]O)=[C:4]([C:10]([F:13])([F:12])[F:11])[CH:3]=1.P(Br)(Br)[Br:15].C(=O)([O-])O.[Na+]>C(Cl)Cl>[Br:15][CH2:8][C:5]1[CH:6]=[CH:7][C:2]([I:1])=[CH:3][C:4]=1[C:10]([F:13])([F:12])[F:11]
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 24614Phosphorus tribromideHCID 516892Sodium BicarbonateHCID 66770401(4-Iodo-2-(trifluoromethyl)phenyl)methanol

生成物 1

HCID 667721121-(Bromomethyl)-4-iodo-2-(trifluoromethyl)benzene収率 48.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒3 回

実験手順

To a solution of [4-iodo-2-(trifluoromethyl)phenyl]methanol (2.1 g, 6.95 mmol) in DCM (15 ml) in an ice-water bath was added dropwise a solution of phosphorous tribromide (0.66 ml, 7.00 mmol, Aldrich) in DCM (15 ml). The resulting solution was allowed to warm to ambient temperature and stirred under nitrogen for 2 h. The reaction mixture was poured onto a mixture of ice-water (50 ml) and saturated sodium hydrogen carbonate (50 ml). The biphasic mixture was diluted with DCM (50 ml). The phases were separated and the aqeuous phase washed with DCM (50 ml). The combined organic phases were washed with water (50 ml), dried (MgSO4), filtered and the solvent removed in vacuo to leave 1-(bromomethyl)-4-iodo-2-(trifluoromethyl)benzene as a brown oil (1.24 g).

後処理

  1. customThe phases were separated
  2. washthe aqeuous phase washed with DCM (50 ml)
  3. washThe combined organic phases were washed with water (50 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customthe solvent removed in vacuo

出典と根拠

ORDレコード
ord-58a1c34a813243bfa2fedf082244a046
出典データセット
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08399436B2

反応ノート

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