Thionyl Chloride → HCID 20072181, compound
Reaction equation
[Cl:1][C:2]1[C:10]([I:11])=[C:9]([Cl:12])[C:8]([F:13])=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:16])=O>>[Cl:1][C:2]1[C:10]([I:11])=[C:9]([Cl:12])[C:8]([F:13])=[CH:7][C:3]=1[C:4]([Cl:16])=[O:5]Participants
3
Procedure
10.0 g of 2,4-dichloro-5-fluoro-3-iodo-benzoic acid and 9.5 ml of thionyl chloride are boiled until gas is no longer produced. The remaining thionyl chloride is then stripped off in vacuo. 10.2 g of crude acyl chloride, which can be employed without further purification, remain.
Workup
- customno longer produced
- custom10.2 g of crude acyl chloride, which can be employed without further purification
Sources & evidence
- ORD record
- ord-3286efce92df4b8eac43e9c9d1dfbc1d
- Source dataset
- uspto-grants-1989_07
- Patent number
- US04851160
Reaction notes
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