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Ethanol → Ethyl 6-hydroxy-2-naphthoate

HRID 1790187
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HRID 1790187 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 855576-Hydroxy-2-naphthoic acid

생성물 1

HCID 2769636Ethyl 6-hydroxy-2-naphthoate

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

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%).

후처리

  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

출처 및 근거

ORD 기록
ord-5f1461830198416ea9317c089d13033f
출처 데이터셋
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07071218B2

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