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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634863Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 54183316, compound

https://huagongshe.com/reaction/634863

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 22006951HCID 22006951—
SolventDichloromethaneHCID 6344—
ProductHCID 54183316HCID 5418331684.5%

Reaction Steps

A solution of 1.1 grams (0.002 mole) of N-[4-(2-methyl-2H-tetrazol-5-yl)phenylmethyl]-4-[bis(4-trifluoromethylphenyl)hydroxymethyl]piperidine (Compound 31-prepared in Example 9) in 100 mL of methylene chloride was stirred, and 0.6 gram (excess) of 50-85% 3-chloroperoxybenzoic acid was added. Upon completion of addition, the reaction mixture was stirred at ambient temperature for about one hour. After this time the reaction mixture was washed with an aqueous 10% solution of sodium hydroxide. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, yielding 1.0 gram of N-[4-(2-methyl-2H-tetrazol-5-yl)phenyl-methyl]-4-[bis(4-trifluoromethylphenyl)hydroxymethyl]piperidine N-oxide. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06184234B2
Source datasetuspto-grants-2001_02
ORD IDord-ac37d1b1d2594e79b18bfa960762c2b4
Source noteuspto-grants-2001_02