Thionyl Chloride → 2,6-Dichloro-5-fluoro-3-pyridinecarbonyl chloride
Reaction equation
[Cl:1][C:2]1[N:10]=[C:9]([Cl:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:15])=O>>[Cl:1][C:2]1[N:10]=[C:9]([Cl:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4]([Cl:15])=[O:5]Participants
3
Procedure
A solution of commercially available (Aldrich) 2,6-dichloro-5-fluoronicotinic acid (5.00 g, 23.8 mmol) in thionyl chloride (15 mL) was heated at reflux for 3 h. After cooling, the solution was concentrated in vacuo to give 2,6-dichloro-5-fluoronicotinoyl chloride as a brown oil which was carried on to the next step without further purification. This transformation can also be accomplished using oxalyl chloride with catalytic DMF in place of thionyl chloride.
Workup
- temperatureat reflux for 3 h
- temperatureAfter cooling
- concentrationthe solution was concentrated in vacuo
Sources & evidence
- ORD record
- ord-cdf506a90b2d4b4794c41d9986c9c602
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06677352B1
Reaction notes
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