HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325826Generated: October 27, 2026
Dipropyl disulfide → 5-(2,4-Dichlorophenoxy) 2-(propylthio)phenol
https://huagongshe.com/reaction/325826
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dipropyl disulfide | HCID 12377 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Propyl sulfenyl chloride | HCID 12535950 | — |
| Reactant | 3-(2,4-Dichlorophenoxy)phenol | HCID 12796172 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2,4-Dichlorophenoxy) 2-(propylthio)phenol | HCID 20462839 | — |
Reaction Steps
3-(2,4-Dichlorophenoxy)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 propyl sulfenyl chloride freshly prepared by reacting dipropyl 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-(2,4-dichlorophenoxy) 2-(propylthio)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-27698d89c2ec418693657c42dd830b43 |
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| Source note | uspto-grants-1984_04 |
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