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Triethyl phosphite → HCID 57758712、化合物

HRID 1510354
ノート
印刷プレビュー

反応式

HRID 1510354 の反応式
[CH3:1][C@:2]1([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH2:6][C:5](=[O:7])[N:4]([C@@H:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH3:9])[CH2:3]1.P(OCC)(OCC)[O:24]CC.C[Si]([N-][Si](C)(C)C)(C)C.[Li+]>O1CCCC1>[OH:24][CH:6]1[C:5](=[O:7])[N:4]([C@@H:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH3:9])[CH2:3][C@@:2]1([CH3:1])[C:16]([O:18][C:19]([CH3:21])([CH3:20])[CH3:22])=[O:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 31215Triethyl phosphiteHCID 2733832Lithium hexamethyldisilazaneHCID 577587301,1-Dimethylethyl (3S)-3-methyl-5-oxo-1-[(1R)-1-phenylethyl]-3-pyrrolidinecarboxylate

生成物 1

HCID 57758712HCID 57758712、化合物収率 91.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of tert-butyl (3S)-3-methyl-5-oxo-1-[(1R)-1-phenylethyl]pyrrolidine-3-carboxylate (10.0 g, 33.0 mmol) and triethyl phosphite (6.78 mL, 39.6 mmol) in anhydrous tetrahydrofuran (165 mL), lithium bistrimethylsilylamide (46.1 mL, 46.1 mmol, 1.0M solution in tetrahydrofuran) was added at −5° C., and the mixture was stirred at the same temperature for 30 minutes. After bubbling oxygen gas into the reaction mixture for 2 hours, saturated aqueous solution of ammonium chloride (150 mL) was added to the mixture in an ice bath, and the mixture was concentrated under reduced pressure. Water (100 mL) was added to the residue and the mixture was extracted with ethyl acetate (200 mL×2). The organic layer was washed with saturated aqueous solution of sodium chloride (200 mL), and dried with anhydrous sodium sulfate. After removing the solvent by distillation under reduced pressure, the residue was purified by silica gel column chromatography (hexane : ethyl acetate=1:1→1:4) to obtain 9.61 g (91.3%) of the title compound as a pale yellow oily substance.

後処理

  1. customAfter bubbling oxygen gas into the reaction mixture for 2 hours
  2. additionsaturated aqueous solution of ammonium chloride (150 mL) was added to the mixture in an ice bath
  3. concentrationthe mixture was concentrated under reduced pressure
  4. additionWater (100 mL) was added to the residue
  5. extractionthe mixture was extracted with ethyl acetate (200 mL×2)
  6. washThe organic layer was washed with saturated aqueous solution of sodium chloride (200 mL)
  7. dry with materialdried with anhydrous sodium sulfate
  8. customAfter removing the solvent
  9. distillationby distillation under reduced pressure
  10. customthe residue was purified by silica gel column chromatography (hexane : ethyl acetate=1:1→1:4)

出典と根拠

ORDレコード
ord-657e47c531fc42459aecfbc8f25793be
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08211910B2

反応ノート

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