HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698261Generated: October 29, 2026
Sodium methanesulfinate → HCID 66727614, compound
https://huagongshe.com/reaction/1698261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanesulfinate | HCID 2733271 | — |
| Reactant | HCID 86640807 | HCID 86640807 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 66727614 | HCID 66727614 | — |
Reaction Steps
To a solution of 2-methyl-propane-2-sulfinic acid [(S)-1-(2-bromo-pyridin-4-yl)-ethyl]-amide (3.10 g, 10.2 mmol) (containing 5 wt % of the other diastereomer) in DMSO (120 mL) was added sodium methanesulfinate (3.7 g, 31 mmol) and copper (I) iodide (5.8 g, 31 mmol) The mixture was warmed at 130° C. for 45 minutes. The reaction was diluted with saturated aqueous NH4Cl (90 mL), saturated aqueous NaHCO3 (10 mL), and EtOAc (150 mL), and sonicated for 10 minutes to dissolve all the solids. The aqueous phase was separated and the organic layer was washed with a mixture of saturated aqueous NH4Cl (90 mL) in saturated aqueous NaHCO3 (10 mL). The combined aqueous layers were extracted with EtOAc (150 mL). The combined organic layers were washed with brine, dried over sodium sulfate, filtered and concentrated. The crude material was purified by silica gel chromatography eluting with a gradient of 75-100% EtOAc in hexanes to afford 2-methyl-propane-2-sulfinic acid [(S)-1-(2-methanesulfonyl-pyridin-4-yl)-ethyl]-amide as a clear thick oil as a single diastereomer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163918B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-22d3a5bb7ef0481baf7799da1dea17f7 |
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| Source note | uspto-grants-2012_04 |
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