HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Disulfide → 2-Bromo-5-(methylthio)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Catalyst | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-5-(methylthio)pyridine | HCID 11658494 | 94% |
Reaction Steps
To a solution of 2,5-dibromopyridine (23.4 g, 0.099 mol) in ether (500 mL), n-butyl lithium (1.52 M in n-hexane, 68 mL, 0.10 mmol) was added dropwise at −78° C. and the mixture was stirred for 1 hour at the temperature. Dimethyldisulfide (9.8 mL, 0.11 mol) was added slowly at −78° C. and the mixture was stirred for 1 hour at that temperature and further 1 hour at 0° C. The mixture was quenched with aqueous 1 N hydrochloric acid (200 mL) and extracted with ether (100 mL×2), dried over magnesium sulfate (MgSO4), and concentrated in vacuo gave the title compound (18.9 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06878726B2 |
| Source dataset | uspto-grants-2005_04 |
| ORD ID | ord-2f1358730def43ccbc04d8c5de0f5b89 |
| Source note | uspto-grants-2005_04 |