HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325823Generated: October 25, 2026
Dimethyl Disulfide → 5-(2-Bromo-4-nitrophenoxy)-2-(methylthio)phenol
https://huagongshe.com/reaction/325823
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Methanesulfenylchloride | HCID 138595 | — |
| Reactant | 3-(2-Bromo-4-nitrophenoxy)phenol | HCID 20462806 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(2-Bromo-4-nitrophenoxy)-2-(methylthio)phenol | HCID 20462820 | — |
Reaction Steps
3-(2-Bromo-4-nitrophenoxy)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 methyl sulfenyl chloride freshly prepared by reacting dimethyl disulfide (0.015 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-bromo-4-nitrophenoxy)-2-(methylthio)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-d35bc6de057b45b9a54294f736728743 |
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| Source note | uspto-grants-1984_04 |
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