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

HRID 132624

Reaktionsgleichung

Reaktionsgleichung von HRID 132624
[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]

Komponenten

6

Versuchsvorschrift

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.

Aufarbeitung

  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)

Quellen und Nachweise

ORD-Eintrag
ord-b893801a673040d08b755176e997b607
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07388023B2

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