HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 6-Chloro-3-chloromethyl-4-methoxypyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (6-Chloro-4-methoxypyridazin-3-YL)methanol | HCID 21919279 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-3-chloromethyl-4-methoxypyridazine | HCID 21919294 | — |
Reaction Steps
Excess SOCl2 is added to a stirred solution of (6-chloro-4-methoxy-pyridazin-3-yl)-methanol (140 mg, 0.8 mmol) in CH2Cl2 (4 mL). The reaction mixture is stirred at room temperature for 4 hours. The solvent is removed in vacuo; toluene (4 mL) is added and evaporated to dryness. Flash column chromatography (silica gel) purification of the residue provides 6-chloro-3-chloromethyl-4-methoxy-pyridazine as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122546B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-7dc2075a0418446cb3fd2714965154c1 |
| Source note | uspto-grants-2006_10 |