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Sulfuric Acid → 2-Acetoxy-3-chloro-benzoic acid

HRID 2190906
ノート
印刷プレビュー

反応式

HRID 2190906 の反応式
[OH:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[C:12](OC(=O)C)(=[O:14])[CH3:13].OS(O)(=O)=O>>[C:12]([O:1][C:2]1[C:10]([Cl:11])=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5])(=[O:14])[CH3:13]
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

4

反応物 3

HCID 1118Sulfuric AcidHCID 7918Acetic AnhydrideHCID 745853-Chlorosalicylic acid

生成物 1

HCID 181834362-Acetoxy-3-chloro-benzoic acid収率 94.6%

反応条件

温度
100 °C

実験手順

To a mixture of 2-hydroxy-3-chloro-benzoic acid (5.0 g, 29.0 mmol) in acetic anhydride (9.0 mL, 95.6 mmol) was added conc. H2SO4 (0.44 mL) at rt. Resulting suspension was heated in a 100° C. oil bath for 40 min. After cooled to about 50° C., the reaction mixture was poured onto ice (100 g) with stirring. Liquid was decanted off and the gooey residue was dissolved in methylene chloride, washed with water and brine, and dried over MgSO4. It was then filtered, and concentrated to give the title compound (5.89 g). 1H NMR (200 MHz, CDCl3): δ (ppm)=7.99 (dd, J=7.8, 1.6 Hz, 1H), 7.66 (dd, J=7.8, 1.6 Hz, 1H), 7.28 (m, 1H), 2.39 (s, 3H).

後処理

  1. customResulting suspension
  2. temperatureAfter cooled to about 50° C.
  3. additionthe reaction mixture was poured onto ice (100 g)
  4. customLiquid was decanted off
  5. dissolutionthe gooey residue was dissolved in methylene chloride
  6. washwashed with water and brine
  7. dry with materialdried over MgSO4
  8. filtrationIt was then filtered
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-bbedcedd2850448cbea0c92fba9b1dde
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08324405B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート