Triphenylphosphine → (4S)-4-(acetylsulfanyl)pyrrolidin-2-one

HRID 1030178ノート

反応式

HRID 1030178 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.O[CH:21]1[CH2:25][NH:24][C:23](=[O:26])[CH2:22]1.N(C(OCC)=O)=NC(OCC)=O.[C:39]([OH:42])(=[S:41])[CH3:40]>O1CCCC1>[C:39]([S:41][CH:21]1[CH2:25][NH:24][C:23](=[O:26])[CH2:22]1)(=[O:42])[CH3:40]

参加物

6

実験手順

20-(1) 15.6 g of triphenylphosphine were added to a suspension of 3 g of 4-hydroxy-2-pyrrolidinone in 200 ml of tetrahydrofuran, and then the mixture was stirred at room temperature for 5 minutes, after which it was cooled to -20° C. A solution of 9.3 ml of diethyl azodicarboxylate in 9 ml of tetrahydrofuran was added dropwise, whilst cooling at -12° C. to -20° C., to the previous solution. The mixture was then stirred at 0°-5° C. for 5 minutes, after which it was again cooled to -20° C. 4.2 ml of thioacetic acid were then added dropwise to the mixture, whilst cooling at -18° C. to -20° C. The mixture was then warmed to 0-5° C. and stirred at that temperature for 2 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure. The residue was purified first by column chromatography through silica gel, eluted with a 10:1 by volume mixture of ethyl acetate and methanol, and then by column chromatography through silica gel, eluted with a 2:1 by volume mixture of acetonitrile and benzene, to give 2.45 g of 4-acetylthio-2-pyrrolidinone as colorless crystals.

後処理

  1. temperatureafter which it was cooled to -20° C
  2. temperaturewhilst cooling at -12° C. to -20° C., to the previous solution
  3. stirringThe mixture was then stirred at 0°-5° C. for 5 minutes
  4. temperatureafter which it was again cooled to -20° C
  5. temperaturewhilst cooling at -18° C. to -20° C
  6. temperatureThe mixture was then warmed to 0-5° C.
  7. stirringstirred at that temperature for 2 hours
  8. concentrationAt the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure
  9. customThe residue was purified first by column chromatography through silica gel
  10. washeluted with a 10:1 by volume mixture of ethyl acetate and methanol
  11. washby column chromatography through silica gel, eluted with a 2:1 by volume mixture of acetonitrile and benzene

出典と根拠

ORDレコード
ord-53c68418537144af8ead58a9279c0921
出典データセット
uspto-grants-1992_04
特許番号
US05104867

反応ノート

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