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Ethanol → Ethyl 6-hydroxy-2-naphthoate

HRID 1790187
ノート
印刷プレビュー

反応式

HRID 1790187 の反応式
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([C:12]([OH:14])=[O:13])[CH:6]=[CH:5]2.[CH2:15](O)[CH3:16]>S(=O)(=O)(O)O>[CH2:15]([O:13][C:12]([C:7]1[CH:6]=[CH:5][C:4]2[C:9](=[CH:10][CH:11]=[C:2]([OH:1])[CH:3]=2)[CH:8]=1)=[O:14])[CH3:16]
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 2

HCID 702EthanolHCID 855576-Hydroxy-2-naphthoic acid

生成物 1

HCID 2769636Ethyl 6-hydroxy-2-naphthoate

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

A solution of 6-hydroxy-2-naphthoic acid (75.9 g, 0.40 mol) in ethanol (1.0 L) and sulfuric acid (5.0 mL) was heated to reflux under an atmosphere of nitrogen. After 16 hours, the volume was removed to approximately half via simple distillation and the resulting solution was diluted with water. The resulting cloudy mixture was extracted with EtOAc (4×) and the combined organics were successively washed with NaHCO3 (0.25 M, twice), water, brine and dried (MgSO4). The mixture was filtered and evaporated to give 6-hydroxy-naphthalene-2-carboxylic acid ethyl ester, 85.4 g (98%).

後処理

  1. temperatureto reflux under an atmosphere of nitrogen
  2. customthe volume was removed to approximately half via simple distillation
  3. additionthe resulting solution was diluted with water
  4. extractionThe resulting cloudy mixture was extracted with EtOAc (4×)
  5. washthe combined organics were successively washed with NaHCO3 (0.25 M
  6. dry with materialtwice), water, brine and dried (MgSO4)
  7. filtrationThe mixture was filtered
  8. customevaporated

出典と根拠

ORDレコード
ord-5f1461830198416ea9317c089d13033f
出典データセット
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07071218B2

反応ノート

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