HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537255Generated: October 29, 2026
Methanol → 2-(Benzylthio)-6-(trifluoromethyl)pyridine
https://huagongshe.com/reaction/537255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Fluoro-6-(trifluoromethyl)pyridine | HCID 2736501 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Benzylthio)-6-(trifluoromethyl)pyridine | HCID 72213081 | 69.4% |
Reaction Steps
To a suspension of sodium hydride (0.170 g, 4.24 mmol) in tetrahydrofuran (10 mL) was added phenylmethanethiol (0.338 ml, 2.88 mmol) dropwise at 0° C. The reaction mixture was stirred at 0° C. for 15 minutes then 2-fluoro-6-(trifluoromethyl)pyridine (0.365 ml, 3.03 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 30 minutes. Methanol (1 mL) was added carefully and the reaction mixture was stirred at 0° C. for a further 10 minutes then water (5 mL) and dichloromethane (10 mL) were added. The organic layer was recovered using a phase separator cartridge then concentrated in vacuo to give 2-(benzylthio)-6-(trifluoromethyl)pyridine (538 mg) as a colourless oil. LCMS (Method F, ES-API): RT 2.80 min, m+H=270.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08859774B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-1a762b3af496432996c4594a971641df |
|---|
| Source note | uspto-grants-2014_10 |
|---|