HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium methanethiolate → 5-[1-(Methylthio)ethyl]-2-(trichloromethyl)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 5-(1-Bromoethyl)-2-(trichloromethyl)pyridine | HCID 59218638 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-[1-(Methylthio)ethyl]-2-(trichloromethyl)pyridine | HCID 59218620 | — |
Reaction Steps
A solution of 5-(1-bromoethyl)-2-(trichloromethyl)pyridine (A) (0.95 g, 3.14 mmol) in ethanol (15 mL) was treated with sodium thiomethoxide (0.44 g, 6.29 mmol) portionwise at 0° C. The mixture was stirred at room temperature overnight. The solvent ethanol was then removed under a reduced pressure and the residue was re-taken into CH2Cl2 and brine. The two phases were separated and the organic layer was dried over anhydrous Na2SO4, filtered, concentrated. The residue was purified on silica gel using 5% EtOAc in hexane to give 0.57 g of the partially pure 5-[1-(methylthio)ethyl]-2-(trichloromethyl)pyridine (B) in 67% crude yield. GC-MS: mass calcd for C9H10Cl3NS [M]+ 269. Found 269.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08013164B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-7518dfa8b780492caeac64e0ac6817cc |
| Source note | uspto-grants-2011_09 |