Tert-Butanesulfinamide → HCID 58562506, compound
Reaction equation
[O:1]1[C:5]2([CH2:10][CH2:9][CH:8]([CH:11]=O)[CH2:7][CH2:6]2)[O:4][CH2:3][CH2:2]1.[CH3:13][C:14]([S:17]([NH2:19])=[O:18])([CH3:16])[CH3:15]>C1COCC1.C(OCC)(=O)C.[O-]CC.[Ti+4].[O-]CC.[O-]CC.[O-]CC>[O:4]1[C:5]2([CH2:6][CH2:7][CH:8](/[CH:11]=[N:19]/[S:17]([C:14]([CH3:16])([CH3:15])[CH3:13])=[O:18])[CH2:9][CH2:10]2)[O:1][CH2:2][CH2:3]1Participants
Procedure
To a solution of 1,4-dioxaspiro[4.5]decane-8-carbaldehyde (6.68 g, 39.2 mmol, prepared as described in Pearson, et al. in J. Org. Chem. 1997, 62(16), 5284-5292), racemic 2-methylpropane-2-sulfinamide (3.50 g, 28.0 mmol), tech grade titanium (IV) ethoxide (14 mL, 67.5 mmol) were dissolved in dry THF (100 mL), placed under an argon atmosphere and stirred at ambient temperature for 16 hours. The next day the reaction mixture was diluted with ethyl acetate and poured onto rapidly stirred ice cold brine. The copious white precipitate was removed by filtration through celite and the organic layer removed. After drying over Na2SO4 and concentration the residue was purified by flash chromatography (silica gel, 0-100% ether/DCM) to afford the product.
Workup
- additionpoured onto rapidly stirred ice cold brine
- customThe copious white precipitate was removed by filtration through celite
- customthe organic layer removed
- dry with materialAfter drying over Na2SO4 and concentration the residue
- customwas purified by flash chromatography (silica gel, 0-100% ether/DCM)
- customto afford the product
Sources & evidence
- ORD record
- ord-50a3fe017b624b66a99afea57fc6186f
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09062048B2
Reaction notes
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