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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074929Generated: November 1, 2026

m-Chloroperbenzoic acid → Hydrochloric Acid

https://huagongshe.com/reaction/1074929

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-{[(Pentafluorophenyl)sulfanyl]methyl}pyridine--hydrogen chloride (1/1)HCID 12760224—
SolventDichloromethaneHCID 6344—
ProductHydrochloric AcidHCID 313584.2%
Product2-[(2,3,4,5,6-Pentafluorobenzene-1-sulfinyl)methyl]pyridineHCID 12760233—

Reaction Steps

A stirred suspension of 2-(((pentafluorophenyl)thio)methyl)pyridine, hydrochloride (2.0 g) in methylene chloride (50 ml) at 0° C. was treated portionwise with m-chloroperoxybenzoic acid (1.41 g) over 1/2 hour. The mixture was allowed to warm to ambient temperature, sufficient methylene chloride was added to form a solution, and the mixture was stirred a further 1/2 hour. The solution was washed with saturated Na2CO3 solution and water, dried (MgSO4) and evaporated. The residue was converted into the hydrochloride in acetone with ethereal HCl solution to give the title compound, hydrochloride (1.3 g) mp 154°-6° C. (Found: C,41.6; H,2.15; N,3.8 C12H6F5NOS.HCl requires C41.9; H,2.05; N,4.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04394509
Source datasetuspto-grants-1983_07
ORD IDord-2de23493f3bc4819afde4f6cf29ef202
Source noteuspto-grants-1983_07