HuagongsheHuagongshe Chemistry Print Report · For research reference only
Uridine → 362-43-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Uridine | HCID 6029 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 362-43-6 | HCID 351234 | 84% |
Reaction Steps
Para-toluene sulfonic acid (2.33 g, 12.3 mmoles, 3 eq.) was added to Uridine (1 g, 4.1 mmoles) in 180 mL of anhydrous acetone. After 4 hours at room temperature, acetone was evaporated and the residual crude product was dissolved in 200 mL of ethyl acetate. The organic phase was washed three times with 20 mL of a hydrogenocarbonate 10% solution, then dried over sodium sulfate. The solvent was removed under vacuum. 0.979 g of white powder was isolated (Yield: 83%). The characterization data were consistent with the chemical structure and formula.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507859B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-fdd2e929ff174c07be39ed838a27fc28 |
| Source note | uspto-grants-2009_03 |