Methanol → HCID 59599757, compound
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([OH:11])[CH:2]=1.[OH-:12].[Na+].ClCCl.[CH3:17]O>C(Cl)(Cl)Cl.O>[OH:11][C:3]1[CH:2]=[N:1][C:10]2[C:5]([C:4]=1[CH:17]=[O:12])=[CH:6][CH:7]=[CH:8][CH:9]=2Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 100 °C
Procedure
Quinolin-3-ol (500 mg, 3.44 mmol, 1.0 eq) is added at room temperature to a stirred solution of sodium hydroxide (1.6 g, 40.0 mmol, 11.6 eq) in chloroform (1 mL) and water (10 mL). After 2 hours stirring at 100° C., the reaction mixture is extracted with dichloromethane (3×20 mL) and water (20 mL) and the pH is adjusted to 4 by the addition of a 1N hydrochloric acid aqueous solution. The combined organic layers are dried over sodium sulfate, filtered and concentrated to give a residue that is purified by column chromatography (silica gel, eluent: dichloromethane:methanol, 200:1, v/v) to afford 3-hydroxy-quinoline-4-carbaldehyde as a yellow solid (60 mg, 10% yield).
Workup
- extractionthe reaction mixture is extracted with dichloromethane (3×20 mL) and water (20 mL)
- additionthe pH is adjusted to 4 by the addition of a 1N hydrochloric acid aqueous solution
- dry with materialThe combined organic layers are dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- customto give a residue that
- customis purified by column chromatography (silica gel, eluent
Sources & evidence
- ORD record
- ord-92ed5703c3594770934508b436bae49e
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09120822B2
Reaction notes
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