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Iodine → 2-Bromo-1-iodo-3-(trifluoromethyl)benzene

HRID 1422609
ノート
印刷プレビュー

反応式

HRID 1422609 の反応式
N([O-])=O.[Na+].[Br:5][C:6]1[C:12]([C:13]([F:16])([F:15])[F:14])=[CH:11][CH:10]=[CH:9][C:7]=1N.OS(O)(=O)=O.[I:22]I.[O-]S([O-])=O.[Na+].[Na+]>O>[Br:5][C:6]1[C:12]([C:13]([F:16])([F:15])[F:14])=[CH:11][CH:10]=[CH:9][C:7]=1[I:22]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 807IodineHCID 1118Sulfuric AcidHCID 24437Sodium SulfiteHCID 940582-Bromo-3-(trifluoromethyl)anilineHCID 23668193Sodium Nitrite

生成物 1

HCID 534844702-Bromo-1-iodo-3-(trifluoromethyl)benzene

試薬・触媒・溶媒 1

HCID 962
Water
溶媒
3 回

反応条件

温度
40 °C

実験手順

An ice-cold solution of NaNO2 (0.15 g) in water (0.5 mL) is added to a mixture of 2-bromo-3-trifluoromethyl-aniline (0.48 g), concentrated H2SO4 (2 mL), and water (1.8 mL) at ca. 5° C. The mixture is stirred in the cooling bath for 20 min and then poured into a solution of KI (0.56 g) and I2 (0.56 g) in water (0.5 mL). After gas evolution ceases, the mixture is heated to 40° C. and stirred at this temperature for 1 h. The mixture is cooled to room temperature and aqueous Na2SO3 solution is added. The resulting mixture is extracted with ethyl acetate, and the combined extracts are dried (Na2SO4) and concentrated. The solvent is evaporated and the residue is chromatographed (cyclohexane/ethyl acetate 95:5→90:10) to give the title compound.

後処理

  1. stirringstirred at this temperature for 1 h
  2. temperatureThe mixture is cooled to room temperature
  3. extractionThe resulting mixture is extracted with ethyl acetate
  4. dry with materialthe combined extracts are dried (Na2SO4)
  5. concentrationconcentrated
  6. customThe solvent is evaporated
  7. customthe residue is chromatographed (cyclohexane/ethyl acetate 95:5→90:10)

出典と根拠

ORDレコード
ord-381a02c6b88d4df79d9454cce2a87247
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08927531B2

反応ノート

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