HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534987Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 66792841, compound
https://huagongshe.com/reaction/534987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 66792717 | HCID 66792717 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66792841 | HCID 66792841 | 88% |
Reaction Steps
A mixture of 2-[4-(2-tert-butylphenyl)piperazin-1-yl]-2-oxo-N-(tetrahydro-2H-thiopyran-4-yl)acetamide (Example 193, 0.21 g, 0.54 mmol) and m-chloroperbenzoic acid (0.29 g, 1.13 mmol) in ethyl acetate (10 mL) was stirred at 0° C. for 2 h. Then the mixture was added saturated NaHSO3 solution and stirred for 1 h. The mixture was poured into saturated NaHCO3 solution and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate 60:40 to 0:100 then ethyl acetate/methanol 100/0 to 70/30) to give the title compound (0.20 g, 88%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853215B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-2e52bfd2bbe74502a87326152c80e174 |
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| Source note | uspto-grants-2014_10 |
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