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2-Iodobenzoic acid → 2-[(4-Fluorophenyl)sulfanyl]benzoic acid

HRID 2049865
ノート
印刷プレビュー

反応式

HRID 2049865 の反応式
I[C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C(=O)([O-])[O-].[K+].[K+].[F:17][C:18]1[CH:23]=[CH:22][C:21]([SH:24])=[CH:20][CH:19]=1>[N+](C1C=CC=CC=1)([O-])=O.[Cu]>[F:17][C:18]1[CH:23]=[CH:22][C:21]([S:24][C:2]2[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=2[C:4]([OH:6])=[O:5])=[CH:20][CH:19]=1
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

6

反応物 3

HCID 69412-Iodobenzoic acidHCID 11430Potassium Carbonate3 回HCID 677894-Fluorothiophenol

生成物 1

HCID 144187682-[(4-Fluorophenyl)sulfanyl]benzoic acid

試薬・触媒・溶媒 2

HCID 23978Copper触媒HCID 7416Nitrobenzene溶媒

反応条件

温度
160 °C

実験手順

A mixture of 147 g of iodobenzoic acid, 45.5 g of potassium carbonate in 57 ml of nitrobenzene is maintained with stirring at 160° C. for 40 minutes. Thereafter, 46.5 g of additional potassium carbonate which is followed by the addition of 73.1 g of 4-fluorothiophenol, another 46.5 g of potassium carbonate and 0.35 g of copper powder. The reaction mixture is stirred in a 160° C. bath for 45 minutes. The resulting solid is collected and then cooled to 0° C. before being mixed with 100 ml of water and 220 ml of 6 N hydrochloric acid. The aqueous mixture is then diluted to 1 liter total volume before being stirred with 450 ml of chloroform. The resulting white solid is collected and washed successively with chloroform and water. The solid is dissolved in hot acetone and the acetone solution is successively filtered and cooled to provide a white crystalline product. The product is recrystallized from acetone and then converted to a salt with potassium carbonate. The salt is dissolved in water and the aqueous solution acidified with 1 N hydrochloric acid to provide 2-(4-fluorophenylthio)benzoic acid.

後処理

  1. temperatureis maintained
  2. stirringThe reaction mixture is stirred in a 160° C. bath for 45 minutes
  3. customThe resulting solid is collected
  4. temperaturecooled to 0° C.
  5. additionbefore being mixed with 100 ml of water and 220 ml of 6 N hydrochloric acid
  6. additionThe aqueous mixture is then diluted to 1 liter total volume
  7. stirringbefore being stirred with 450 ml of chloroform
  8. customThe resulting white solid is collected
  9. washwashed successively with chloroform and water
  10. dissolutionThe solid is dissolved in hot acetone
  11. filtrationthe acetone solution is successively filtered
  12. temperaturecooled
  13. customto provide a white crystalline product
  14. customThe product is recrystallized from acetone
  15. dissolutionThe salt is dissolved in water

出典と根拠

ORDレコード
ord-c5410c7a8d1c413284e544acc4108e84
出典データセット
uspto-grants-1980_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04198419

反応ノート

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