HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869751Generated: October 29, 2026
Benzyl mercaptan → 3-Methyl-5-[(phenylmethyl)thio]pyridine
https://huagongshe.com/reaction/869751
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Bromo-5-methylpyridine | HCID 817713 | — |
| Catalyst | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Methyl-5-[(phenylmethyl)thio]pyridine | HCID 58349834 | 95.4% |
Reaction Steps
To a solution of 3-bromo-5-methylpyridine (888 mg) in toluene (10 mL) were added phenylmethanethiol (705 mg), N,N-diisopropylethylamine (1.47 g), tris(dibenzylideneacetone)dipalladium(0)(189 mg) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (239 mg), and the mixture was stirred under an argon atmosphere at 80° C. for 1.5 hr. The reaction mixture was filtered through silica gel, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:hexane-ethyl acetate=19:1→17:3) to give the title compound as a yellow oil (yield 1.06 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08969387B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-01be7e513fd24331a04a9123dd9eaf0a |
|---|
| Source note | uspto-grants-2015_03 |
|---|