tert-Butylsulfinamide, (S)-(-)- → (S)-2-Methyl-propane-2-sulfinic Acid ((3S)-1,3-dimethyl-pentylidene)-amide

HRID 132624

反応式

HRID 132624 の反応式
[CH3:1][C@@H:2]([CH2:7][CH3:8])[CH2:3][C:4](=O)[CH3:5].[CH3:9][C:10]([S@@:13]([NH2:15])=[O:14])([CH3:12])[CH3:11]>C1COCC1.[Cl-].[Na+].O.[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC>[CH3:5][C:4](=[N:15][S@:13]([C:10]([CH3:12])([CH3:11])[CH3:9])=[O:14])[CH2:3][C@@H:2]([CH3:1])[CH2:7][CH3:8]

参加物

6

実験手順

A mixture of (S)-4-methyl-hexan-2-one (1.6 g, 14 mmol), (S)-2-methyl-propane-2-sulfinic acid amide (1.7 g, 14 mmol) and titanium(IV) ethoxide (6.4 g, 28 mmol) in THF (30 mL) was refluxed for 10 hours. Then the reaction mixture was poured into brine (150 mL). The mixture was filtered. The filtrate was extracted by EtOAc (3×70 mL). The EtOAc phase was removed under reduce pressure and the residue was purified by a silica gel column (Hexane/EtOAc 3:1) to give the titled compound (1.93 g, 63% yield) as a colorless oil: 1H NMR (CDCl3) δ 2.24 (m, 2H), 2.27 (s, 3H), 1.85 (m, 1H), 1.22 (m, 2H), 1.20 (s, 9H), 0.85 (m, 6H); MS (APCI) (M+1)+ 218.1.

後処理

  1. temperaturewas refluxed for 10 hours
  2. filtrationThe mixture was filtered
  3. extractionThe filtrate was extracted by EtOAc (3×70 mL)
  4. customThe EtOAc phase was removed
  5. customthe residue was purified by a silica gel column (Hexane/EtOAc 3:1)

出典と根拠

ORDレコード
ord-b893801a673040d08b755176e997b607
出典データセット
uspto-grants-2008_06
特許番号
US07388023B2

関連ノート

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