Thionyl Chloride → HCID 86696919, compound
Reaction equation
[C:1]1([N:7]2[C:12](=[O:13])[N:11]([CH3:14])[C:10](=[O:15])[C:9]([C:16]([OH:18])=O)=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:21])=O>>[C:1]1([N:7]2[C:12](=[O:13])[N:11]([CH3:14])[C:10](=[O:15])[C:9]([C:16]([Cl:21])=[O:18])=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Intermediate e (3 g, 0.012 mol) was added to thionyl chloride (10V/W, 30 mL). The mixture was warmed up to react under reflux for 6 h. The solvent was evaporated off to produce a clear yellow crystal (2.8 g) in a yield of 87.5%.
Workup
- temperatureThe mixture was warmed up
- customto react
- temperatureunder reflux for 6 h
- customThe solvent was evaporated off
Sources & evidence
- ORD record
- ord-3ace713c6dec4862bfafd89796939644
- Source dataset
- uspto-grants-2014_09
- Patent number
- US08822465B2
Reaction notes
Loading…