Sodium Hydroxide → 6-Methylquinolin-3-OL

HRID 1835551Notes

Reaction equation

HRID 1835551 reaction equation
N[C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([CH3:12])=[CH:7][CH:6]=2.N([O-])=[O:14].[Na+].[OH-].[Na+]>OS(O)(=O)=O.O>[OH:14][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][C:8]([CH3:12])=[CH:7][CH:6]=2

Participants

6

Reactant 3

HCID 14798Sodium HydroxideHCID 221488796-Methylquinolin-3-amineHCID 23668193Sodium Nitrite

Product 1

HCID 221488886-Methylquinolin-3-OLYield 29%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 1118Sulfuric AcidSolvent2×

Procedure

A solution of 3-Amino-6-methylquinoline [(1.21 g, 7.65 mmol), prepared according to J. Chem. Soc. 2024-2027 (1948) Morley, J. S.; Simpson, J. C. E.] in 6N H2SO4 (25 ml) was cooled in an ice bath. To the solution NaNO2 (560 mg, 8.10 mmol) in water (2 ml) was added and stirred for 30 min at 0 degrees. Separately 5% H2SO4 was refluxed and above Diazo reaction mixture was added to this refluxing solution. After 30 min the reaction mixture was cooled to room temperature, and was neutralized by 6N NaOH. The resulting insoluble material was collected by filtration. This solid was recrystallized by CHCl3/AcOEt to afford compound (308) (348 mg, 29%).

Workup

  1. additionwas added to this refluxing solution
  2. filtrationThe resulting insoluble material was collected by filtration
  3. customThis solid was recrystallized by CHCl3/AcOEt

Sources & evidence

ORD record
ord-6dd7adc282264905a6373f98a9bd052d
Source dataset
uspto-grants-2004_08
Patent number
US06770648B2

Reaction notes

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