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Acetic Acid → 2,4-Bis(trifluoromethyl)phenylacetic acid

HRID 1781252
ノート
印刷プレビュー

反応式

HRID 1781252 の反応式
[F:1][C:2]([F:16])([F:15])[C:3]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[CH:7][C:4]=1[C:5]#N.OS(O)(=O)=O.O.[C:23]([OH:26])(=[O:25])C>>[F:1][C:2]([F:16])([F:15])[C:3]1[CH:10]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:8]=[CH:7][C:4]=1[CH2:5][C:23]([OH:26])=[O:25]
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

5

反応物 4

HCID 176Acetic AcidHCID 962WaterHCID 1118Sulfuric AcidHCID 27361172,4-Bis(trifluoromethyl)benzonitrile

生成物 1

HCID 27361722,4-Bis(trifluoromethyl)phenylacetic acid

反応条件

温度
120 °C

実験手順

2,4-Bis(trifluoromethyl)benzonitrile (41.5 mmol, 10.51 g) was taken up in 100 mL acetic acid, 50 mL conc. H2SO4, and 20 mL water. This was heated to 120° C. for 3 h. The reaction was then diluted with 1 L ice water, and extracted with 2×300 mL ethyl acetate. The combined organics were washed with 2×200 mL water, dried with brine and Na2SO4, and evaporated under reduced pressure. The residue was taken up in a minimum of diethyl ether and crystallized by adding sufficient hexane to precipatate the product. The solid was collected to give 7.74 g of 2,4-bis(trifluoromethyl) phenyl acetic acid as white crystals, 68.5%. NMR 1H (CDCl3) δ 7.93 (s, 1H), 7.80 (d, J=7.9 Hz,1H), 7.55 (d, J=7.9 Hz, 1H), 3.94 (s, 2H).

後処理

  1. extractionextracted with 2×300 mL ethyl acetate
  2. washThe combined organics were washed with 2×200 mL water
  3. dry with materialdried with brine and Na2SO4
  4. customevaporated under reduced pressure
  5. customcrystallized
  6. additionby adding sufficient hexane
  7. customThe solid was collected

出典と根拠

ORDレコード
ord-6d72a2c9c9c844b7b0c5df8ca422b9cd
出典データセット
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05633251

反応ノート

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