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Acetic Acid → HCID 494700、化合物

HRID 1797431
ノート
印刷プレビュー

反応式

HRID 1797431 の反応式
[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]
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

6

反応物 5

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

生成物 1

HCID 494700HCID 494700、化合物収率 39%

反応条件

温度
74 °C

実験手順

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%).

後処理

  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

出典と根拠

ORDレコード
ord-cba995dfadf2449dbdf9926330e9be3c
出典データセット
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07034152B2

反応ノート

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