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Acetic Acid → HCID 494700, 화합물

HRID 1797431
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HRID 1797431 반응식
[O:1]1[C:5](=[O:6])[CH2:4][C@H:3]2[CH:7]=[CH:8][CH2:9][C@@H:2]12.[CH2:10]=O.S(=O)(=O)(O)O.[C:17]([O-:20])(=[O:19])[CH3:18].[Na+].[C:22]([OH:25])(=[O:24])[CH3:23]>>[C:17]([O:20][CH:8]1[CH2:9][CH:2]2[O:1][C:5](=[O:6])[CH2:4][CH:3]2[CH:7]1[CH2:10][O:24][C:22](=[O:25])[CH3:23])(=[O:19])[CH3:18]
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참가 물질

6

반응물 5

HCID 176Acetic AcidHCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 517045Sodium AcetateHCID 110734123,3a,6,6a-Tetrahydro-2H-cyclopenta[b]furan-2-one

생성물 1

HCID 494700HCID 494700, 화합물수율 39%

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온도
74 °C

실험 절차

To a 100 mL round bottomed flask was charged (3aS, 6aR)-3, 3a, 6, 6a-tetrahydro-2H-cyclopenta[b]furan-2-one 49 (3.85 g, 31 mmol, prepared as described in Corey et al. J. Med Chem. 1993, 36, 243), paraformaldehyde (3.0 g), glacial acetic acid (30 mL), and concentrated sulfuric acid (1 mL). The mixture was heated to 74° C. for 24 hours. To the solution was added sodium acetate (4 g). The solution was concentrated in vacuo and the residue was dissolved in ethyl acetate (200 mL). The solution was washed with saturated sodium bicarbonate solution until no gas evolution was observed. The organic phase was dried over sodium sulfate and concentrated in vacuo to give the crude product (4.1 g). The crude product was purified by silica gel column chromatography to provide the title compound (3.1 g, 39%).

후처리

  1. concentrationThe solution was concentrated in vacuo
  2. dissolutionthe residue was dissolved in ethyl acetate (200 mL)
  3. washThe solution was washed with saturated sodium bicarbonate solution until no gas evolution
  4. dry with materialThe organic phase was dried over sodium sulfate
  5. concentrationconcentrated in vacuo
  6. customto give the crude product (4.1 g)
  7. customThe crude product was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-cba995dfadf2449dbdf9926330e9be3c
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07034152B2

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