HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542772Generated: October 31, 2026
Hydrochloric Acid → 3-Bromo-2-(methylthio)benzo[b]thiophene
https://huagongshe.com/reaction/542772
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 2,3-Dibromo-1-benzothiophene | HCID 94977 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Bromo-2-(methylthio)benzo[b]thiophene | HCID 20207244 | — |
Reaction Steps
A solution of 8.76 g of 2,3-dibromobenzo[b]thiophene in 75 ml of diethyl ether was cooled to 0° C. and 19 ml of a 1.6M solution of n-butyl lithium in hexane and 10 ml of diethyl ether were added. A pink slurry formed which was stirred for one hour. A solution of 2.7 ml of methyl disulfide in 10 ml of diethyl ether was added and the reaction mixture was stirred for 4 hours at 0° C. Approximately 100 ml of 1N hydrochloric acid were added and the reaction was allowed to warm to room temperature. The layers were separated and the aqueous layer was extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate and evaporated to dryness. The resulting oil was vacuum distilled at 1.5 torr providing 1 g of the desired subtitled intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04659717 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-8e012850c99649039112604970465041 |
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| Source note | uspto-grants-1987_04 |
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