HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Di-tert-butyl (2R,3R)-2-hydroxy-3-{[5-oxido-4-(phenylsulphonyl)-1,2,5-oxadiazol-3-yl]-oxy}-succinate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Di-tert-butyl tartrate | HCID 281630 | — |
| Reactant | 3,4-Di(benzenesulfonyl)-2-oxo-1,2,5lambda~5~-oxadiazole | HCID 12405466 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Di-tert-butyl (2R,3R)-2-hydroxy-3-{[5-oxido-4-(phenylsulphonyl)-1,2,5-oxadiazol-3-yl]-oxy}-succinate | HCID 67316492 | — |
Reaction Steps
50% NaOH solution (1.2 g-30 mmol) is added in the course of ½ hour to a solution of 3,4-bis(phenylsulphonyl)-1,2,5-oxadiazole 2-oxide (7 g-19 mmol) and di-tert-butyl tartrate (5 g-19 mmol) in 100 ml of anhydrous THF. After stirring for 5 hours, the solvent is evaporated off to dryness and the residue is taken up in water and ethyl acetate. The organic fraction is dried with Na2SO4 and evaporated to dryness and subsequently purified by flash chromatography, using a (98:2) dichloromethane/ethanol mixture as eluant, to yield the expected product in the form of a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981920B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-a19f08ad42c346d288993ad217c62249 |
| Source note | uspto-grants-2011_07 |