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Methanol → Methyl 4-chloro-3-(trifluoromethyl)benzoate

HRID 534255
ノート
印刷プレビュー

反応式

HRID 534255 の反応式
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[C:11]([F:14])([F:13])[F:12].S(=O)(=O)(O)O.[CH3:20]O>>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH3:20])=[O:7])=[CH:4][C:3]=1[C:11]([F:12])([F:13])[F:14]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 27738574-Chloro-3-(trifluoromethyl)benzoic acid

生成物 1

HCID 14148738Methyl 4-chloro-3-(trifluoromethyl)benzoate

実験手順

To a solution of 4-chloro-3-(trifluoromethyl)benzoic acid (10.37 g, 46.2 mmol) in methanol (100 mL) was added concentrated sulfuric acid (0.51 mL, 9.24 mmol). The mixture was heated under reflux overnight. The mixture was allowed to cool to room temperature and concentrated under reduced pressure to form a solid. The solid was filtered and washed with water. The solid was then stirred with saturated aqueous sodium bicarbonate solution to remove any residual sulfuric acid, filtered and dried under vacuum to give the title compound as a white solid (10.18 g). 1H NMR (400 MHz, CDCl3) δ ppm 3.96 (s, 3H), 7.60 (d, J=8.34 Hz, 1H), 8.14 (dd, J=8.34, 2.02 Hz, 1H), 8.37 (d, J=2.02 Hz, 1H).

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux overnight
  3. concentrationconcentrated under reduced pressure
  4. customto form a solid
  5. filtrationThe solid was filtered
  6. washwashed with water
  7. customto remove any residual sulfuric acid
  8. filtrationfiltered
  9. customdried under vacuum

出典と根拠

ORDレコード
ord-aefca7bd3e3948499b80a87a5c39a1f2
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08853419B2

反応ノート

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