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Allyl Alcohol → HCID 67157178、化合物

HRID 549470
ノート
印刷プレビュー

反応式

HRID 549470 の反応式
CC([O:4][CH2:5][C@H:6]1[O:11][C@H:10]([O:12][C:13]([CH3:15])=O)[C@H:9]([O:16]C(C)=O)[C@@H:8]([O:20]C(C)=O)[C@@H:7]1[O:24][C@@H:25]1[O:30][C@H:29]([CH2:31][O:32]C(C)=O)[C@@H:28]([O:36]C(C)=O)[C@H:27]([O:40]C(C)=O)[C@H:26]1[O:44]C(C)=O)=O.[CH2:48](O)C=C.FC(F)(F)S(O[Si](C)(C)C)(=O)=O.C[O-].[Na+]>C(Cl)Cl.O>[C@@H:25]1([O:24][C@@H:7]2[C@@H:6]([CH2:5][OH:4])[O:11][CH:10]([O:12][CH2:13][CH:15]=[CH2:48])[C@H:9]([OH:16])[C@H:8]2[OH:20])[O:30][C@H:29]([CH2:31][OH:32])[C@@H:28]([OH:36])[C@H:27]([OH:40])[C@H:26]1[OH:44]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 7858Allyl AlcoholHCID 65367Trimethylsilyl triflateHCID 111065Alpha-D-cellobiose octaacetateHCID 10942334Sodium Methoxide

生成物 1

HCID 67157178HCID 67157178、化合物収率 91%

試薬・触媒・溶媒 2

HCID 962
Water
溶媒
HCID 6344Dichloromethane溶媒

実験手順

α-D-cellobiose octaacetate (48.59 g, 71.6 mmol) was dissolved in methylene chloride (600 mL), and allyl alcohol (29 ml, 0.43 mol) and trimethylsilyl trifluoromethanesulfonate (16 mL, 86.0 mmol) were added thereto under ice-cooling, followed by stirring of the mixture at room temperature for 1.5 hours. Water (200 mL) was added to the reaction mixture and the mixture was extracted with methylene chloride (200 mL). The extract was washed with a saturated aqueous NaCl solution (100 mL) and after it was dried with anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was dissolved in methanol (300 mL) and sodium methoxide (28 mL, 0.14 mol) was added thereto under ice-cooling, followed by stirring of the mixture at room temperature for 2 hours. Dowex 50w×8 was added to the reaction mixture until the reaction mixture became neutral and after it was filtered, the solvent was distilled off under reduced pressure. The residue was purified using silica gel flash column chromatography (ethyl acetate:methanol:water, 8:2:1, V/V) to obtain the desired title compound (24.8 g, yield: 91%) as a pale yellow amorphous substance.

後処理

  1. temperatureunder ice-cooling
  2. extractionthe mixture was extracted with methylene chloride (200 mL)
  3. washThe extract was washed with a saturated aqueous NaCl solution (100 mL)
  4. dry with materialafter it was dried with anhydrous sodium sulfate
  5. distillationthe solvent was distilled off under reduced pressure
  6. dissolutionThe residue was dissolved in methanol (300 mL)
  7. temperatureunder ice-cooling
  8. stirringby stirring of the mixture at room temperature for 2 hours
  9. filtrationafter it was filtered
  10. distillationthe solvent was distilled off under reduced pressure
  11. customThe residue was purified

出典と根拠

ORDレコード
ord-981fb77af59c4009bfc118677cd954fc
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07943584B2

反応ノート

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