HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Chloro-2-chloromethyl-3,5-dimethylpyridinium chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (4-Chloro-3,5-dimethylpyridin-2-YL)methanol | HCID 9795246 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-2-chloromethyl-3,5-dimethylpyridinium chloride | HCID 68539750 | — |
Reaction Steps
To a solution of 4-chloro-2-hydroxymethyl-3,5-dimethylpyridine (60.7 g, 354 mmol) and DMF (0.25 mL, 3.54 mmol) in toluene (200 mL) was added thionyl chloride (26.9 mL, 371 mmol) over 2 h at 15-30° C. After stirring for 2 more h at ambient temperature, ethanol (6 mL) was added to the thick slurry. The solids were filtered off at about 10° C., washed with toluene (80 mL) and dried at 40° C. in vacuo to give 4-chloro-2-chloromethyl-3,5-dimethylpyridinium chloride as an off-white solid (m. p. 195-196° C.); yield 66.5 g (84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601737B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-151d3854aefa45b982e22f6bcd61b1c8 |
| Source note | uspto-grants-2009_10 |