Sodium Thiosulfate → HCID 89975559, compound
Reaction equation
CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C1=CC=CC=2)=O.[CH3:23][S:24]([O:27][C@@H:28]([C@@H:30]1[C@H:34]([CH2:35][OH:36])[O:33][C:32]([CH3:38])([CH3:37])[O:31]1)[CH3:29])(=[O:26])=[O:25].C(=O)([O-])O.[Na+].S([O-])([O-])(=O)=S.[Na+].[Na+]>ClCCl.C(OCC)(=O)C.N1C=CC=CC=1>[CH3:23][S:24]([O:27][C@@H:28]([C@@H:30]1[C@H:34]([CH:35]=[O:36])[O:33][C:32]([CH3:37])([CH3:38])[O:31]1)[CH3:29])(=[O:25])=[O:26]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Procedure
3 g of 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3 (1H)-one (Dess-Martin Periodinane) was added to a solution of 1.8 g of (1R)-1-((4S,5S)-5-(hydroxymethyl)-2,2-dimethyl-1,3-dioxolane-4-yl)ethyl methanesulfonate (which contained fluorotris(propan-2-yl)silane) and 1.16 mL of pyridine in 20 mL of dichloromethane at a temperature of 5° C. to 10° C., and the obtained mixture was then stirred at room temperature for 2 hours. Thereafter, ethyl acetate, a saturated sodium hydrogen carbonate aqueous solution and a sodium thiosulfate aqueous solution were added to the reaction mixture. The organic layer was fractionated, and it was successively washed with water and a saturated sodium chloride aqueous solution and was then dried over anhydrous magnesium sulfate. The solvent was distilled away under reduced pressure, so as to obtain 1.7 g of (1R)-1-((4S,5R)-5-formyl-2,2-dimethyl-1,3-dioxolane-4-yl)ethyl methanesulfonate in the form of a yellow oily product.
Workup
- washit was successively washed with water
- dry with materiala saturated sodium chloride aqueous solution and was then dried over anhydrous magnesium sulfate
- distillationThe solvent was distilled away under reduced pressure
Sources & evidence
- ORD record
- ord-ae614910996f426a9453adb281acb89d
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221865B2
Reaction notes
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