HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325825Generated: October 30, 2026
Diethyl disulfide → HCID 20462832, compound
https://huagongshe.com/reaction/325825
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl disulfide | HCID 8077 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | HCID 11608460 | HCID 11608460 | — |
| Reactant | ethanesulfenyl chloride | HCID 12275523 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20462832 | HCID 20462832 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04443248 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-71b96314bf3941488a18f13edd0f077d |
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| Source note | uspto-grants-1984_04 |
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