HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Methyl 4-chloro-6-(chloromethyl)pyridine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Methyl 4-chloro-6-(hydroxymethyl)pyridine-2-carboxylate | HCID 14083517 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4-chloro-6-(chloromethyl)pyridine-2-carboxylate | HCID 68456565 | — |
Reaction Steps
To a solution of methyl 4-chloro-6-(hydroxymethyl)-2-pyridinecarboxylate (166 mg, Ref: Kittika et al., Tetrahedron, 44 (10), 2821, (1988)) in dry dichloromethane (3 ml) was added thionyl chloride (66 μl). The solution was stirred for 40 minutes. LC/MS indication reaction completion. Solvent was removed u.r.p. (under reduced pressure) to give a white solid. Toluene (˜2 ml) added then removed u.r.p. The residue was dried in vacuo to give a white solid. (175 mg, 97%). LC/MS [MH+]=220/222, Rt=2.51 min. Title compound obtained as the free base.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07759369B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-e23950b542e54805a0240b04517cfd5e |
| Source note | uspto-grants-2010_07 |