Thionyl Chloride → HCID 86696919, compound
Reaction equation
[C:1]1([N:7]2[C:12](=[O:13])[N:11]([CH2:14]CCC)[C:10](=[O:18])[C:9]([C:19]([OH:21])=O)=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:24])=O>>[C:1]1([N:7]2[C:12](=[O:13])[N:11]([CH3:14])[C:10](=[O:18])[C:9]([C:19]([Cl:24])=[O:21])=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Intermediate g (3.0 g, 0.01 mol) was added to thionyl chloride (10 V/W, 30 mL). The mixture was warmed up under stirring to react under reflux for 6 h. The solvent was evaporated off to produce a clear yellow crystal (3 g) in a yield of 88%,
Workup
- temperatureThe mixture was warmed up
- customto react
- temperatureunder reflux for 6 h
- customThe solvent was evaporated off
Sources & evidence
- ORD record
- ord-66cfc52be7f44c119ffa045b572da6f6
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08993566B2
Reaction notes
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