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Water → (2S,4R)-1-benzyl-2-vinyl-4-(t-butyldimethylsilyloxy)pyrrolidine

HRID 975654
ノート
印刷プレビュー

反応式

HRID 975654 の反応式
[CH3:1]C(C)([O-])C.[K+].[CH2:7]([N:14]1[CH2:18][C@H:17]([O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21])[CH2:16][C@H:15]1[CH:27]=O)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O.C(OCC)(=O)C>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C1(C)C=CC=CC=1.CCCCCC>[CH2:7]([N:14]1[CH2:18][C@H:17]([O:19][Si:20]([C:23]([CH3:26])([CH3:25])[CH3:24])([CH3:22])[CH3:21])[CH2:16][C@H:15]1[CH:27]=[CH2:1])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=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 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 23665647Potassium tert-butoxideHCID 50922891(2S,4R)-1-benzyl-2-formyl-4-(t-butyldimethylsilyloxy)pyrrolidine

生成物 1

HCID 11726876(2S,4R)-1-benzyl-2-vinyl-4-(t-butyldimethylsilyloxy)pyrrolidine収率 83.7%

試薬・触媒・溶媒 3

HCID 74505
Methyltriphenyliphosphonium bromide
触媒
HCID 1140Toluene溶媒
HCID 8058Hexane溶媒

実験手順

To a suspension of methyltriphenylphosphonium bromide (1.07 g) was portionwise added potassium t-butoxide (337 mg) with stirring under ice-cooling. The mixture was stirred at ambient temperature for 2 hours. To the solution cooled on ice-bath was added dropwise (2S,4R)-1-benzyl-2-formyl-4-(t-butyldimethylsilyloxy)pyrrolidine (0.92 g) in toluene (2 ml) and the mixture was stirred at the same temperature for 1 hour. The reaction mixture was poured into a mixture of water (10 ml) and ethyl acetate (20 ml). The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo to give a residue. To the residue was added n-hexane (30 ml). The resulting precipitates were filtered off and the filtrate was evaporated in vacuo. The resulting residue was chromatographed on silica gel (1 g) eluting with a mixture of n-hexane and ethyl acetate (5:1 v/v). The fractions containing the desired compound were collected and evaporated in vacuo to give (2S,4R)-1-benzyl-2-vinyl-4-(t-butyldimethylsilyloxy)pyrrolidine (765 mg).

後処理

  1. temperaturecooling
  2. stirringThe mixture was stirred at ambient temperature for 2 hours
  3. temperatureTo the solution cooled on ice-bath
  4. stirringthe mixture was stirred at the same temperature for 1 hour
  5. customThe organic layer was separated
  6. washwashed with saturated aqueous sodium chloride
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customevaporated in vacuo
  9. customto give a residue
  10. customThe resulting precipitates
  11. filtrationwere filtered off
  12. customthe filtrate was evaporated in vacuo
  13. customThe resulting residue was chromatographed on silica gel (1 g)
  14. washeluting with a mixture of n-hexane and ethyl acetate (5:1 v/v)
  15. additionThe fractions containing the desired compound
  16. customwere collected
  17. customevaporated in vacuo

出典と根拠

ORDレコード
ord-273dfd43d3a74f128e203cba9feace52
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05608056

反応ノート

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