HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (3R,3aS,6R,6aR)-6-Hydroxyhexahydrofuro[3,2-b]furan-3-yl 4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | (3R,3aS,6R,6aR)-hexahydro-furo[3,2-b]furan-3,6-diol | HCID 7269354 | — |
| Product | (3R,3aS,6R,6aR)-6-Hydroxyhexahydrofuro[3,2-b]furan-3-yl 4-methylbenzenesulfonate | HCID 13014014 | — |
Reaction Steps
A solution of 5 g of (3R,3aS,6R,6aR)-hexahydro-furo[3,2-b]furan-3,6-diol in 50 ml of pyridine is stirred for 16 h with 7.8 g of toluenesulfonylchloride. From the mixture obtained solvent is distilled off and the distillation residue obtained is dissolved in EtAc and extracted with 1N HCl, saturated aqueous NaHCO3-solution and H2O. The organic layer obtained is dried, solvent is evaporated and the evaporation residue is subjected to chromatography. Toluene-4-sulfonic acid (3R, 3aS,6R,6aR)-6-hydroxy-hexahydro-furo[3,2-b]furan-3-yl ester is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088823B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-a44d2e1e38004f2081f010fb22461f1e |
| Source note | uspto-grants-2012_01 |