HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764588Generated: November 1, 2026
Dimethyl Disulfide → HCID 20285731, compound
https://huagongshe.com/reaction/1764588
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 2,4-Dibromo-3,5-dimethylthiophene | HCID 10588076 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20285731 | HCID 20285731 | — |
Reaction Steps
20.0 G. of 2,4-dibromo-3,5-dimethylthiophene was dissolved in 300 ml. of anhydrous ehtyl ether. The resulting solution was cooled to -70° C. with stirring under argon. 32 Ml. of a 2.4 M solution of n-butyl lithium was added slowly and the solution was warmed to -32° C. for 10 minutes and then cooled again to -70° C. 7.5 G. of dimethyldisulfide was added slowly while the temperature was maintained at -70° C. The resulting solution was warmed to room temperature and stirred for 2 hours then poured into ice water, stirred for 15 minutes, and extracted with ethyl ether. The combined ether extracts were washed with water, 5% sodium carbonate, and saturated sodium chloride solution; dried over sodium sulfate, filtered and evaporated to yield 3-bromo-2,4-dimethyl-5-(methylthio)thiophene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04116975 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-516d178426fd4dc684522e854458e6c9 |
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| Source note | uspto-grants-1978_09 |
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