Methane, tris(methylthio)- → (4S)-1-(t-butyldimethylsilyl)-4-(2,2,2-tri(methylthio)ethyl)azetidin-2-one

HRID 1105515ノート

反応式

HRID 1105515 の反応式
C([Li])CCC.[CH3:6][S:7][CH:8]([S:11][CH3:12])[S:9][CH3:10].[Si:13]([N:20]1[C@H:23]([CH2:24]I)[CH2:22][C:21]1=[O:26])([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]>C1COCC1>[Si:13]([N:20]1[C@H:23]([CH2:24][C:8]([S:11][CH3:12])([S:9][CH3:10])[S:7][CH3:6])[CH2:22][C:21]1=[O:26])([C:16]([CH3:19])([CH3:18])[CH3:17])([CH3:15])[CH3:14]

参加物

5

反応物 3

HCID 138491Methane, tris(methylthio)-HCID 12944335(4S)-1-(t-butyldimethylsilyl)-4-iodomethyl-azetidin-2-oneHCID 178418339Butyllithium

生成物 1

HCID 13003464(4S)-1-(t-butyldimethylsilyl)-4-(2,2,2-tri(methylthio)ethyl)azetidin-2-one収率 82%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

n-Butyllithium (19.4 ml of 2.5 M hexane solution, 48.5 mmol) is added slowly by syringe to a solution of tri(methylthio)methane (7.47 g, 48.5 mmol) in 150 ml of freshly distilled THF at -78° C. The resulting solution is stirred at -78° C. for 30 min. prior to the addition of a solution of (4S)-1-(tert-butyldimethylsilyl)-4-iodomethylazetidin-2-one (15.0 g, 46.15 mmol) in 50 ml of THF. This solution is stirred at -78° C. for 30 min., then quenched by addition of saturated aqueous ammonium chloride solution. The reaction mixture is allowed to warm to room temperature, then poured into ether (250 ml), washed with water (2×100 ml) brine (100 ml) and dried over magnesium sulfate. Removal of solvents in vacuo gives an oil which is crystallized from petroleum ether to give 13.3 g (82%) of (4S)-1-(t-butyldimethylsilyl)-4-(2,2,2-tri(methylthio)ethyl)azetidin-2-one as colorless prisms. m.p. 61°-62° C. IR(CHCl3, CM-1) 2918, 2850, 1730; n.m.r. (CDCl3) δ 4.0(m,l), δ 3.35(dd,l,J=5.5,16), δ 2,83 (dd,l,J=3,16) δ 2,5(ABq,2) δ 2,15(s, 9), δ 0.98(s,9), δ0.25(s,6).

後処理

  1. stirringThis solution is stirred at -78° C. for 30 min.
  2. customquenched by addition of saturated aqueous ammonium chloride solution
  3. temperatureto warm to room temperature
  4. additionpoured into ether (250 ml)
  5. washwashed with water (2×100 ml) brine (100 ml)
  6. dry with materialdried over magnesium sulfate
  7. customRemoval of solvents in vacuo
  8. customgives an oil which
  9. customis crystallized from petroleum ether

出典と根拠

ORDレコード
ord-f0d5a43d7ee8431daa0e37776616f040
出典データセット
uspto-grants-1982_01
特許番号
US04309346

反応ノート

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