HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247485Generated: October 27, 2026
Phthalimide potassium salt → (5R)-2-[3-(3-fluoro-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dione
https://huagongshe.com/reaction/1247485
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | (5R)-3-(3-Fluorophenyl)-5-[[(methylsulfonyl)oxy]methyl]-2-oxazolidinone | HCID 46912058 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (5R)-2-[3-(3-fluoro-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dione | HCID 68535606 | 91.8% |
Reaction Steps
A solution of mesylate 97 (2.89 g, 10.0 mmol) in anhydrous DMF (20 mL) was treated with solid potassium phthalimide (2.22 g, 70.0 mmol, 1.2 equiv) at 25° C., and the resulting reaction mixture was warmed to 70° C. for 4 h. When TLC and HPLC showed the reaction was complete, the reaction mixture was cooled to room temperature before being quenched with H2O (60 mL). The resulting mixture was stirred at room temperature for 10 min before being cooled to 0–5° C. for 1 h. The white precipitate was collected by filtration, washed with water (2×40 mL), and dried in vacuo to afford the desired (5R)-2-[3-(3-fluoro-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-isoindole-1,3-dione (phthalimide 98, 3.12 g, 91.8% yield) as an off-white powder. This product was directly used in subsequent reactions without further purification. C18H13FN2O4, LCMS (EI) m/e 341 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129259B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-2edda15c6f56409086287986c35f4743 |
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| Source note | uspto-grants-2006_10 |
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