HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484411Generated: October 30, 2026
Sodium methanethiolate → 5-Bromo-2-methylsulfanylmethyl-pyridine
https://huagongshe.com/reaction/1484411
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 5-bromo-2-(chloromethyl)pyridine | HCID 11401501 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-2-methylsulfanylmethyl-pyridine | HCID 115622354 | 81% |
Reaction Steps
To the stirred solution of 5-Bromo-2-chloromethyl-pyridine (3.5 gm, 16.99 mmol) in DMF (25 mL) at 0° C. is added Sodium thiomethoxide (1.31 gm, 18.68 mmol) resulting reaction mixture is stirred at 0° C. for 2 h. After completion quenched with water and extracted with ethyl acetate (3×100 mL). The Combined organic layer is washed with brine and organic layer dried over sodium sulphate, evaporate under reduced pressure. The crude is purified by column chromatography using silica 100-200 mesh using 10% EtOAc: Hexane as eluent to afford title compound (3 g) as brown colored liquid. 1NMR (400 MHz, DMSO) δ: 2.00 (s, 3H), 3.75 (s, 2H), 7.39 (d, J=8.32 Hz, 1H), 7.99-8.02 (dd, J1=2.44 Hz, J2=8.32 Hz, 1H), 8.60 (d, J=2.28 Hz, 1H). LC-MS (m/z): M+H=220.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422236B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-d131c5f4e7c041d196a4c2ed5a1a6949 |
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| Source note | uspto-grants-2016_08 |
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