HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885318Generated: November 1, 2026
Sodium methanesulfinate → {3-[4-Methanesulfonyl-2-((4S,5R)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid methyl ester
https://huagongshe.com/reaction/885318
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | {3-[4-Bromo-2-((4S,5R)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid methyl ester | HCID 58237509 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | {3-[4-Methanesulfonyl-2-((4S,5R)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid methyl ester | HCID 58237649 | 97.5% |
Reaction Steps
{3-[4-Bromo-2-((4S,5R)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-4-methoxy-phenyl}-acetic acid methyl ester (0.1 g, 0.19 mmol), sodium methanesulfinate (0.087 g, 0.84 mmol), and copper iodide (0.159 g, 0.84 mmol) were combined in NMP (2 mL) and degassed with N2 for 10 minutes. The reaction was then stirred at 150° C. for 3 hours, until no starting material was seen by analytical tlc. The mixture was filtered through Celite and worked-up with brine and EtOAc, and the crude material was purified by silica gel chromatography to give the desired product as a colorless oil (0.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242145B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-907f8b68cf2c4c57bb5f964b65631520 |
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| Source note | uspto-grants-2012_08 |
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