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Methanol → (3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid methyl ester

HRID 1157212
ノート
印刷プレビュー

反応式

HRID 1157212 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:10][C:11]([OH:13])=[O:12])[CH:5]=[C:6]([CH3:9])[C:7]=1[OH:8].S(=O)(=O)(O)O.[CH3:19]O>>[CH3:19][O:12][C:11](=[O:13])[CH2:10][C:4]1[CH:5]=[C:6]([CH3:9])[C:7]([OH:8])=[C:2]([Cl:1])[CH:3]=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

4

反応物 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 68441962(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid

生成物 1

HCID 68444019(3-Chloro-4-hydroxy-5-methyl-phenyl)-acetic acid methyl ester収率 91%

反応条件

温度
70 °C

実験手順

A solution of (3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid (5b) (1.4 g, 6.98 mmol) in methanol (60 mL) was treated with concentrated sulfuric acid (0.5 mL) at room temperature under argon. The reaction mixture was heated to 70° C. for 24 h. At this time, the reaction mixture was concentrated under vacuum. The resulting oil was diluted with ethyl acetate (100 mL). The organics were washed with water (2×50 mL), dried with magnesium sulfate, filtered and concentrated. The resulting residue was purified by column chromatography using silica gel eluted with 10% ethyl acetate in petroleum ether to afford 3-chloro-4-hydroxy-5-methyl-phenyl)-acetic acid methyl ester (6b) (1.36 g, 91%) as a white solid; EI(+)-HRMS m/z calcd for C10H11ClO3 (M+) 214.0397, found 214.0400. Molecular Weight=214.6504; Exact Mass=214.0397

後処理

  1. concentrationAt this time, the reaction mixture was concentrated under vacuum
  2. additionThe resulting oil was diluted with ethyl acetate (100 mL)
  3. washThe organics were washed with water (2×50 mL)
  4. dry with materialdried with magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe resulting residue was purified by column chromatography
  8. washeluted with 10% ethyl acetate in petroleum ether

出典と根拠

ORDレコード
ord-34ebab68b3b648cdba77cc3e57530762
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07807674B2

反応ノート

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