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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534987Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 66792841, compound

https://huagongshe.com/reaction/534987

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 66792717HCID 66792717—
SolventEthyl AcetateHCID 8857—
ProductHCID 66792841HCID 6679284188%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-2e52bfd2bbe74502a87326152c80e174
Source noteuspto-grants-2014_10