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Metaperiodic acid → HCID 10828821、化合物

HRID 1953050
ノート
印刷プレビュー

反応式

HRID 1953050 の反応式
I(O)(=O)(=O)=[O:2].C(OC([N:13]1[C@@H:17]([CH2:18][OH:19])[CH2:16][C@@H:15]([C:20]2[CH:25]=[CH:24][C:23]([O:26][CH2:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)=[CH:22][CH:21]=2)[C:14]1=[O:34])=O)(C)(C)C>C(#N)C.C(Cl)Cl.[O-2].[O-2].[O-2].[Cr+6].I(O)(=O)(=O)=O.[O-2].[O-2].[O-2].[Cr+6]>[CH2:27]([O:26][C:23]1[CH:22]=[CH:21][C:20]([C@H:15]2[C:14](=[O:34])[NH:13][C@@H:17]([C:18]([OH:2])=[O:19])[CH2:16]2)=[CH:25][CH:24]=1)[C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1
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

7

反応物 2

HCID 65185Metaperiodic acidHCID 69921464HCID 69921464、化合物

生成物 1

HCID 10828821HCID 10828821、化合物

試薬・触媒・溶媒 4

HCID 10219390chromium (VI) trioxide触媒HCID 131721976Periodic acid chromium trioxide触媒HCID 6342Acetonitrile溶媒
2 回
HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

A solution containing 6.0 g of periodic acid and chromium trioxide (13 mg) in wet acetonitrile (60 mL; 0.75 volume % water) was prepared. A portion of this solution (15 mL) was added dropwise to a solution of (3S,5R)-3-(4-benzyloxyphenyl)-5-hydroxymethyl-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester (1.02 g, 2.57 mmol) in wet acetonitrile (15 mL; 0.75 volume % water) at 0° C. The reaction mixture was stirred at 0° C. for 2 hours. At this time, more of the periodic acid/chromium trioxide solution (5 mL) was added. Stirring at 0° C. was continued for an additional 1 hour. After quenching with a solution of dibasic sodium phosphate (720 mg) in water (12 mL), the mixture was extracted twice with diethyl ether. The combined organic extracts were washed with aqueous sodium bisulfite solution (440 mg in 10 mL water) and brine. After drying over MgSO4, the solvent was evaporated to provide a yellow solid that was taken up in methylene chloride (100 mL) and cooled in an ice bath. Hydrogen chloride gas was bubbled through the cold solution for 2 minutes and the resulting mixture was stirred at 0° C. for 1 hour. The solvent and HCl were evaporated to afford a solid from which the title compound, 226 mg (28%) was isolated by trituration with a mixture of methylene chloride, diethyl ether and ethyl acetate. The trituration filtrate was dissolved in aqueous saturated NaHCO3 solution and washed twice with diethyl ether. After careful acidification with aqueous 6M HCl solution, the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and concentrated to provide more of the title compound, 123 mg (15%).

後処理

  1. customwas prepared
  2. stirringStirring at 0° C.
  3. waitwas continued for an additional 1 hour
  4. customAfter quenching with a solution of dibasic sodium phosphate (720 mg) in water (12 mL)
  5. extractionthe mixture was extracted twice with diethyl ether
  6. washThe combined organic extracts were washed with aqueous sodium bisulfite solution (440 mg in 10 mL water) and brine
  7. dry with materialAfter drying over MgSO4
  8. customthe solvent was evaporated
  9. customto provide a yellow solid that
  10. temperaturecooled in an ice bath
  11. customHydrogen chloride gas was bubbled through the cold solution for 2 minutes
  12. stirringthe resulting mixture was stirred at 0° C. for 1 hour
  13. customThe solvent and HCl were evaporated

出典と根拠

ORDレコード
ord-23cd943f293c41019210023ca9a782a6
出典データセット
uspto-grants-2000_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06114361

反応ノート

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