HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712779Generated: October 29, 2026
Sodium methanethiolate → HCID 68756332, compound
https://huagongshe.com/reaction/712779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 3-Bromo-5-(bromomethyl)pyridine | HCID 14932948 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68756332 | HCID 68756332 | 91.7% |
Reaction Steps
3-Bromo-5-bromomethyl-pyridine (7.5 g, 30 mmol) is dissolved in EtOH (200 mL). The solution is cooled down to 0° C. Sodium thiomethoxide (3.1 g, 45 mmol) is added slowly and the reaction mixture is stirred for 16 hrs. Then the solvent is removed, water and EtOAc are added. The aqueous layer is separated and extracted with EtOAc. Organic layers are combined and concentrated to give 6.0 g of the 3-bromo-5-methylsulfanylmethyl-pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181272B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-75ccd43aaee64bffbd201e16328c53a8 |
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| Source note | uspto-grants-2015_11 |
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