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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042003Generated: October 29, 2026

m-Chloroperbenzoic acid → HCID 59577235, compound

https://huagongshe.com/reaction/2042003

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 59577054HCID 59577054—
SolventEthyl AcetateHCID 8857—
ProductHCID 59577235HCID 5957723554%

Reaction Steps

A solution of 2-({2-[4-(2-tert-butyl-4-fluorophenoxy)piperidin-1-yl]-2-oxoethyl}sulfanyl)phenol (292 mg, 0.70 mmol) obtained in Example 239 and m-chloroperbenzoic acid (275 mg, 1.12 mmol) in ethyl acetate (14 mL) was stirred at 0° C. for 3 hr. Saturated aqueous sodium bisulfite solution (5 mL) was added to the reaction mixture, and the mixture was stirred at room temperature for 30 min. The reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate 90:10-20:80) to give 2-({2-[4-(2-tert-butyl-4-fluorophenoxy)piperidin-1-yl]-2-oxoethyl}sulfinyl)phenol (163 mg, 54%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586571B2
Source datasetuspto-grants-2013_11
ORD IDord-0b3b5fa643ed4e3c9a50bac09d1b3edf
Source noteuspto-grants-2013_11