Sodium Thiosulfate → HCID 89975559, compound

HRID 1508655Notes

Reaction equation

HRID 1508655 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

8

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

  1. washit was successively washed with water
  2. dry with materiala saturated sodium chloride aqueous solution and was then dried over anhydrous magnesium sulfate
  3. 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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