HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Chloro-3-methoxy-4-vinyl-6-(1-chloroethyl)-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 18799939 | HCID 18799939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-3-methoxy-4-vinyl-6-(1-chloroethyl)-pyridine | HCID 18799787 | 92.1% |
Reaction Steps
A solution of 2-chloro-3-methoxy-4-vinyl-6-(1-hydroxyethyl)-pyridine (446 mg, 2.09 mmol) in 10 mL of methylene chloride at 0° C. is treated with thionyl chloride (0.227 mL, 3.13 mmol) and stirred at room temperature for 1 h. The reaction is quenched with 15 mL of saturated sodium bicarbonate. The aqueous layer is extracted with 3×10 mL of methylene chloride. The combined organics are dried over potassium carbonate and concentrated in vacuo to provide 447 mg (92%) of 2-chloro-3-methoxy-4-vinyl-6-(1-chloroethyl)-pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043248 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-1d551c35b1cc4323b8710edd95fbe3ac |
| Source note | uspto-grants-2000_03 |