HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711391Generated: November 1, 2026
2-Bromopyridine → HCID 13058732, compound
https://huagongshe.com/reaction/711391
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | HCID 21224760 | HCID 21224760 | — |
| Solvent | Formamide | HCID 713 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13058732 | HCID 13058732 | 65% |
Reaction Steps
A solution of (4-bromophenyl)(trichloromethyl)sulfane (0.25 g, 0.816 mmol) in 12 mL of formamide was degassed with nitrogen and treated with 2-bromopyridine (0.078 ml, 0.816 mmol). The reaction solution was heated at 75° C. overnight. Then it was cooled to room temperature and diluted with water, extracted with DCM, dried over sodium sulfate, filtered and concentrated. The crude product was purified by column chromatography on silica gel, eluted with 1-5% of EtOAc in 20% DCM/heptanes (v/v), affording 0.14 g (65% yield) of 2-((4-bromophenyl)thio)pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181270B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-074fbe53de2f44449cd64b3e25233c2d |
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| Source note | uspto-grants-2015_11 |
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