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Dimethyl Sulfoxide → tert-Butyl(R)-1-benzyloxycarbonyl-3-methyl-4-oxopyrrolidine-3-carboxylate

HRID 229521
ノート
印刷プレビュー

反応式

HRID 229521 の反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[CH2:11]([O:18][C:19]([N:21]1[CH2:25][CH:24]([OH:26])[C@:23]([CH3:34])([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:22]1)=[O:20])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C.[Cl-].[NH4+]>ClCCl.O>[CH2:11]([O:18][C:19]([N:21]1[CH2:25][C:24](=[O:26])[C@:23]([CH3:34])([C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[CH2:22]1)=[O:20])[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 679Dimethyl SulfoxideHCID 8471TriethylamineHCID 25517Ammonium ChlorideHCID 65578Oxalyl chlorideHCID 68864468tert-butyl(R)-1-benzyloxycarbonyl-4-hydroxy-3-methylpyrrolidine-3-carboxylate

生成物 1

HCID 68861931tert-Butyl(R)-1-benzyloxycarbonyl-3-methyl-4-oxopyrrolidine-3-carboxylate
収率 85.8%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6344Dichloromethane溶媒3 回

実験手順

To a solution of oxalyl chloride (1.01 mL, 11.7 mmol) in dichloromethane (40 mL), a solution of dimethyl sulfoxide (1.11 mL, 15.6 mmol) in dichloromethane (5 mL) was added at −78° C., and the mixture was stirred for 10 minutes. After adding a solution of tert-butyl(R)-1-benzyloxycarbonyl-4-hydroxy-3-methylpyrrolidine-3-carboxylate (1.97 g, 5.87 mmol) in dichloromethane (15 mL) and stirring the mixture for 1 hour, triethylamine (5.98 mL, 42.9 mmol) was added, and the mixture was stirred −78° C. for 30 minutes and in an ice bath for 30 minutes. To the reaction mixture were added saturated aqueous solution of ammonium chloride (50 mL) and water (100 mL), and the mixture was extracted with ethyl acetate (200 mL×2). The organic layer was washed with water (100 mL) and saturated aqueous solution of sodium chloride (100 mL), and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate=10:1→3:2) to obtain 1.68 g (85.8%) of the title compound as a colorless oily substance.

後処理

  1. stirringstirring the mixture for 1 hour
  2. stirringthe mixture was stirred −78° C. for 30 minutes and in an ice bath for 30 minutes
  3. extractionthe mixture was extracted with ethyl acetate (200 mL×2)
  4. washThe organic layer was washed with water (100 mL) and saturated aqueous solution of sodium chloride (100 mL)
  5. dry with materialdried with anhydrous sodium sulfate
  6. customThe solvent was removed by distillation under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (hexane-ethyl acetate=10:1→3:2)

出典と根拠

ORDレコード
ord-5919e72d2b054452a36c3ed36730be58
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07563805B2

反応ノート

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