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Hydrochloric Acid → 4-Chloro-2-iodo-6-methylphenol

HRID 1468472
ノート
印刷プレビュー

反応式

HRID 1468472 の反応式
[CH3:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[OH:9].[Na+].[I-:11].[OH-].[Na+].[O-]Cl.[Na+].[O-]S([O-])(=S)=O.[Na+].[Na+].Cl>CO>[I:11][C:4]1[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([CH3:1])[C:3]=1[OH:9]
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

8

反応物 6

HCID 313Hydrochloric AcidHCID 5238Sodium IodideHCID 14798Sodium HydroxideHCID 148554-Chloro-2-methylphenolHCID 24477Sodium ThiosulfateHCID 23665760Sodium Hypochlorite

生成物 1

HCID 513419354-Chloro-2-iodo-6-methylphenol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

To a stirred solution of 5.00 g (35.00 mmol) of 2-methyl-4-chlorophenol (available from Aldrich Chemical Company) in 100 mL of methanol at 0° C., add 6.83 g (45.57 mmol) of NaI and 1.40 g (35.00 mmol) of NaOH. To the resulting mixture add 65 mL of 5% aqueous NaOCl solution (commercial bleach) over one hour period. The resulting slurry is stirred for one more hour at 0° C. After the addition of 20 mL of 10% Na2S2O3 solution, the reaction mixture is acidified by dilute hydrochloric acid. The mixture is extracted with methylene chloride. The organic layer is washed with brine and dried over anhydrous magnesium sulfate. Removal of the solvent followed by purification by recrystallization from hexanes gives 3.80 g (40.5%) of (P11) as white solid.

後処理

  1. extractionThe mixture is extracted with methylene chloride
  2. washThe organic layer is washed with brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customRemoval of the solvent
  5. customfollowed by purification by recrystallization from hexanes
  6. customgives 3.80 g (40.5%) of (P11) as white solid

出典と根拠

ORDレコード
ord-33149b301a4e478483b43ff10eb715cf
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09000108B2

反応ノート

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