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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534986Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 66750969, compound

https://huagongshe.com/reaction/534986

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 66792717HCID 66792717—
SolventEthyl AcetateHCID 8857—
ProductHCID 66750969HCID 6675096955%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-[4-(2-tert-butylphenyl)piperazin-1-yl]-2-oxo-N-(tetrahydro-2H-thiopyran-4-yl)acetamide (Example 193, 0.25 g, 0.63 mmol), in ethyl acetate (5 mL) was added m-chloroperbenzoic acid (0.19 g, 0.76 mmol) at 0° C. After stirred at 0° C. for 3 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 50:50 to 0:100 then ethyl acetate/methanol 100/0 to 70/30) to give the title compound (0.14 g, 55%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853215B2
Source datasetuspto-grants-2014_10
ORD IDord-3f8ce4aa606948e68ebf264465144c84
Source noteuspto-grants-2014_10