Thionyl Chloride → HCID 14774174, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][CH:21]=1)[C:16](O)=[O:17].S(Cl)([Cl:24])=O>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][O:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][CH:21]=1)[C:16]([Cl:24])=[O:17]Participants
3
Procedure
A mixture of 15.6 g (0.1 mol) of 3-(2-quinolinylmethyloxy)benzoic acid and 11.9 g (0.1 mol) of thionyl chloride is refluxed for 4 hours. The reaction mixture is then evaporated to dryness at room temperature and used directly in the next step.
Workup
- temperatureis refluxed for 4 hours
- customThe reaction mixture is then evaporated to dryness at room temperature
Sources & evidence
- ORD record
- ord-02c8fd29c27644149bfc81e3ec948c8f
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06376512B1
Reaction notes
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