HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ciprofloxacin (R)-5-Oxotetrahydrofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ciprofloxacin | HCID 2764 | — |
| Reactant | (R)-5-oxo-2-tetrahydrofurancarboxylic acid | HCID 104532 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ciprofloxacin (R)-5-Oxotetrahydrofuran-2-carboxylate | HCID 86749208 | 84.3% |
Reaction Steps
0.781 G (0.006 mole) of (R)-5-oxotetrahydrofuran-2-carboxylic acid and 1.99 g (0.006 mole) of Ciprofloxacin were added to 10 mL of distilled water. The resulting mixture was stirred for 30 minutes to dissolve it completely. After adding 20 mL of anhydrous acetone, the resulting solution was further stirred for 30 minutes under ice-cooling and allowed to stand to precipitate solids. The precipitated solids were filtered under reduced pressure through a filter paper (Whatman Filter Paper No. 1), washed three times with each 30 mL of anhydrous acetone, and dried under vacuum to give 2.33 g of the titled compound as white solids. M.P. 211-212° C. (decomposition) [α]D25 =+4.72 (H2O)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05484785 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-5d8ff55fc1224d86a785b7fcd3626851 |
| Source note | uspto-grants-1996_01 |