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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325830Generated: October 25, 2026

Dimethyl Disulfide → 5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenol

https://huagongshe.com/reaction/325830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl DisulfideHCID 12232—
ReactantChlorineHCID 24526—
ReactantMethanesulfenylchlorideHCID 138595—
Reactant3-(2-Cyano-4-fluorophenoxy)phenolHCID 20462842—
SolventDichloromethaneHCID 6344—
Product5-(2-Cyano-4-fluorophenoxy)-2-methylthiophenolHCID 20462834—
Product5-(2-Cyano-4-fluorophenoxy) 2-(methylthio)phenolHCID 20462849—

Reaction Conditions

Temperature-20 °C

Reaction Steps

3-(2-Cyano-4-fluorophenoxy)phenol (0.1 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 methyl sulfenyl chloride freshly prepared by reacting dimethyl 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-cyano-4-fluorophenoxy) 2-(methylthio)phenol as the residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04443248
Source datasetuspto-grants-1984_04
ORD IDord-9bd8d7f06934470fbb7d5f2a826628a1
Source noteuspto-grants-1984_04