Sodium Hydroxide → HCID 178432242, 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]=[C:4]([CH3:16])[C:3]=1[C:17]([O:19]CC)=[O:18].[OH-].[Na+]>>[OH:1][C:2]1[C:11]2[C:6](=[C:7]([C:12]([F:15])([F:13])[F:14])[CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([CH3:16])[C:3]=1[C:17]([OH:19])=[O:18]Participants
3
Procedure
A suspension of 19.4 g of the product of Step B in 162 ml of N sodium hydroxide was refluxed for 5 hours and the mixture was then washed with ether and modified to a pH of 1 with N hydrochloric acid. The mixture was filtered and the solid precipitate was washed with water and dried to obtain 16.6 g of 4-hydroxy-2-methyl-8-trifluoromethyl-quinoline-3-carboxylic acid melting at 260° C.
Workup
- temperaturewas refluxed for 5 hours
- washthe mixture was then washed with ether
- filtrationThe mixture was filtered
- washthe solid precipitate was washed with water
- customdried
Sources & evidence
- ORD record
- ord-67f41d2fa8fa4614b5046864ac509f5c
- Source dataset
- uspto-grants-1978_08
- Patent number
- US04107310
Reaction notes
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