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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378514Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 54183316, compound

https://huagongshe.com/reaction/378514

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 numberUS06030987
Source datasetuspto-grants-2000_02
ORD IDord-35aec2a7dd5f449abe30ca0541ae48fc
Source noteuspto-grants-2000_02