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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325825Generated: October 30, 2026

Diethyl disulfide → HCID 20462832, compound

https://huagongshe.com/reaction/325825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl disulfideHCID 8077—
ReactantChlorineHCID 24526—
ReactantHCID 11608460HCID 11608460—
Reactantethanesulfenyl chlorideHCID 12275523—
SolventDichloromethaneHCID 6344—
ProductHCID 20462832HCID 20462832—

Reaction Conditions

Temperature-20 °C

Reaction Steps

3-(2-chloro-4-cyanophenoxy)phenol (0.01 mole) and methylene chloride (200 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer and addition funnel. The mixture is stirred until dissolved and cooled to about -20° C. A solution of ethyl sulfenyl chloride freshly prepared by reacting diethyl disulfide (0.15 mole) with chlorine (0.18 mole) in methylene chloride (100 ml) is then added dropwise to the reaction vessel over a period of about 40 minutes. After the addition is completed stirring is continued for 30 minutes with cooling and 30 minutes at room temperature. After this time the reaction mixture is washed with water (200 ml), with 5% aqueous sodium bicarbonate (200 ml) and again with water (200 ml). The washed solution is then dried by passing it through a phase separator. The dried solution is stripped of solvent under reduced pressure and the residue chromatographed using a clay column and hexane/ethyl acetate as the eluant. The fractions containing the product are combined and stripped of solvent to yield the desired product 5-(2-chloro-4-cyanophenoxy)-2-(ethylthio)phenol as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443248
Source datasetuspto-grants-1984_04
ORD IDord-71b96314bf3941488a18f13edd0f077d
Source noteuspto-grants-1984_04