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Sulfuric Acid → Ethyl 4-hydroxy-7-methoxy-2-oxo-2',3',5',6'-tetrahydro-spiro[naphthalene-1,4'-pyran]-3-carboxylate

HRID 1868672
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HRID 1868672 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:9]2([C:15]([CH:17]([C:23]([O:25][CH2:26][CH3:27])=[O:24])[C:18]([O:20]CC)=O)=[O:16])[CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1.OS(O)(=O)=O>>[OH:20][C:18]1[C:6]2[C:5](=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)[C:9]2([CH2:14][CH2:13][O:12][CH2:11][CH2:10]2)[C:15](=[O:16])[C:17]=1[C:23]([O:25][CH2:26][CH3:27])=[O:24]
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3

반응물 2

HCID 1118Sulfuric AcidHCID 67099313Diethyl 2-(4-(3-methoxyphenyl)-tetrahydro-2H-pyran-4-carbonyl)malonate

생성물 1

HCID 67099622Ethyl 4-hydroxy-7-methoxy-2-oxo-2',3',5',6'-tetrahydro-spiro[naphthalene-1,4'-pyran]-3-carboxylate수율 29.8%

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온도
0 °C

실험 절차

Diethyl 2-(4-(3-methoxyphenyl)-tetrahydro-2H-pyran-4-carbonyl)malonate (2.1 g, see Example 18) was added to 5 mL H2SO4 stirred at 0° C. The mixture was stirred at room temperature for 1 hour, M+1=379. The mixture was then poured into 100 g crushed ice and extracted with EtOAc (3×50 mL). The combined organic layers were washed with H2O (20 mL) and brine (20 mL), dried over anhydrous Na2SO4, and concentrated in vacuo. The crude product was purified by column chromatography eluting with 20% EtOAc/hexane to give 0.55 g of the title compound. MS (m/z)=379 (M+H)+.

후처리

  1. stirringThe mixture was stirred at room temperature for 1 hour
  2. additionThe mixture was then poured into 100 g
  3. customcrushed ice
  4. extractionextracted with EtOAc (3×50 mL)
  5. washThe combined organic layers were washed with H2O (20 mL) and brine (20 mL)
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated in vacuo
  8. customThe crude product was purified by column chromatography
  9. washeluting with 20% EtOAc/hexane

출처 및 근거

ORD 기록
ord-6f68d3ddd9684b02b3830cb8d30f9fb4
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07635715B2

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