Thionyl Chloride → HCID 23300100, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[C:6]([CH3:13])=[C:5]2[C:14]([OH:16])=O.S(Cl)([Cl:19])=O>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[C:6]([CH3:13])=[C:5]2[C:14]([Cl:19])=[O:16]Participants
3
Procedure
6.5 g (0.027 mol) of the carboxylic acid prepared in Example 1 are dissolved in 80 ml of thionyl chloride and heated under reflux for two hours. For working-up, the reaction mixture is concentrated under reduced pressure on a rotary evaporator and the residue which remains is stirred with diethyl ether. The reaction product is filtered off and the solid obtained is dried in vacuo.
Workup
- temperatureheated
- temperatureunder reflux for two hours
- concentrationthe reaction mixture is concentrated under reduced pressure on a rotary evaporator
- filtrationThe reaction product is filtered off
- customthe solid obtained
- customis dried in vacuo
Sources & evidence
- ORD record
- ord-929bb7a3fc184b19a8c2bd7b05e34e72
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06114349
Reaction notes
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