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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071913Generated: October 29, 2026

Sulfur dichloride → 3,4-Dichlorophenylmethanesulfenyl chloride

https://huagongshe.com/reaction/2071913

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur dichlorideHCID 25353—
Reactant3,4-Dichlorotoluene-alpha-thiolHCID 118986—
ReactantHCID 178526253HCID 178526253—
Product3,4-Dichlorophenylmethanesulfenyl chlorideHCID 21409968—

Reaction Steps

3,4-Dichlorophenylmethanesulfenyl chloride is prepared from the corresponding 3,4-dichlorobenzyl mercaptan in accordance with the procedure of Example I for the preparation of the sulfenyl chloride, except that this reaction is conducted under cooling conditions. The sulfenyl chloride is reacted with the mercaptopyridine-1-oxide as described in Example I, giving an 84% yield of 3,4-dichlorobenzyl 1-oxo-2-pyridyl disulfide having a melting point of 133.0°-134.0° C. and

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04049665
Source datasetuspto-grants-1977_09
ORD IDord-69bfa39ad1c94840afdd79f2dfbe0599
Source noteuspto-grants-1977_09