Thionyl Chloride → HCID 178521124, compound
Reaction equation
[OH:1][C:2]1[C:11]2[C:6](=[C:7]([C:12]([F:15])([F:14])[F:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([OH:18])=O.S(Cl)([Cl:21])=O>>[OH:1][C:2]1[C:11]2[C:6](=[C:7]([C:12]([F:15])([F:14])[F:13])[CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([Cl:21])=[O:18]Participants
3
Procedure
A mixture of 0.5 g of 4-hydroxy-8-trifluoromethyl-3 -quinoline-carboxylic acid in 5 ml of thionyl chloride was stirred at room temperature for 24 hours and the precipitate formed was recovered by vacuum filtration to obtain 0.4 g of 4-hydroxy-8-trifluoromethyl-3-quinoline-carboxylic acid chloride melting at 222° C.
Workup
- customthe precipitate formed
- filtrationwas recovered by vacuum filtration
Sources & evidence
- ORD record
- ord-9c960e990a0e4356ac17dfad6c20d1d2
- Source dataset
- uspto-grants-1976_11
- Patent number
- US03992540
Reaction notes
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