Tert-Butanesulfinamide → HCID 58562506, compound

HRID 2175498Notes

Reaction equation

HRID 2175498 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]1

Participants

6

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

  1. additionpoured onto rapidly stirred ice cold brine
  2. customThe copious white precipitate was removed by filtration through celite
  3. customthe organic layer removed
  4. dry with materialAfter drying over Na2SO4 and concentration the residue
  5. customwas purified by flash chromatography (silica gel, 0-100% ether/DCM)
  6. 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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