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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107395Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 15450553, compound

https://huagongshe.com/reaction/1107395

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 9800792HCID 9800792—
SolventChloroformHCID 6212—
ProductHCID 15450553HCID 15450553—

Reaction Steps

To a dissolved solution of N-(1-benzyl-4-piperidinyl)-2-ethoxy-3-methyl-2-phenylbutanamide (invention compound, Compound No. 1) (400 mg, 1.01 mmole) in chloroform (20 ml) was added 70% m-chloroperbenzoic acid (271 mg, 1.1 mmole). The mixture was stirred at room temperature for 3 days. After the reaction was completed, the reaction mixture was washed with a saturated aqueous sodium bicarbonate solution. The organic layer was dried over anhydrous sodium sulfate. The solvent was then removed under reduced pressure. The residue was purified by a silica gel column to obtain the invention compound (Compound No. 16, 316 mg, 77.0%) were obtained as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06060485
Source datasetuspto-grants-2000_05
ORD IDord-5d7bf41a3e044aa491e611173e873721
Source noteuspto-grants-2000_05