Hydrochloric Acid → HCID 178424441, compound

HRID 1039573Notes

Reaction equation

HRID 1039573 reaction equation
[OH:1][C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[N:4][C:3]=1Cl.[CH:10]1([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([CH3:19])[C:14]=2[OH:20])[CH2:12][CH2:11]1.CC(CCC1C=CC=CC=1)CO.[OH-].[K+].Cl>CO>[Cl:8][C:6]1[N:5]=[N:4][C:3]([O:20][C:14]2[C:15]([CH3:19])=[CH:16][CH:17]=[CH:18][C:13]=2[CH:10]2[CH2:11][CH2:12]2)=[C:2]([OH:1])[CH:7]=1

Participants

7

Reactant 5

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 9834046HCID 9834046, compoundHCID 229399512-Cyclopropyl-6-methylphenolHCID 178516198HCID 178516198, compound

Product 1

HCID 178424441HCID 178424441, compoundYield 66%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a mixture of 302 mg (purity: 100%; 1.83 mmol) of 4-hydroxy-3,6-dichloropyridazine and 826 mg (5.48 mmol) of 2-cyclopropyl-6-methylphenol were added 2-methyl-4-phenylbutanol (2.76 g) and 330 mg (5.60 mmol) of 95% potassium hydroxide at room temperature. The resultant mixture was heated to 180° C. while stirring, and stirred at that temperature for 4 hours. Then, the resultant reaction mixture was cooled to room temperature, and a 1 N aqueous hydrochloric acid solution and methanol were added to the reaction mixture to obtain a uniform solution. The obtained solution was quantitatively determined by an HPLC internal standard analysis method, which showed that 332 mg of 6-chloro-3-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (yield: 66%) and 3.6 mg of 3-chloro-6-(2-cyclopropyl-6-methylphenoxy)-4-pyridazinol (yield: 0.7%) were obtained.

Workup

  1. stirringstirred at that temperature for 4 hours
  2. customThen, the resultant reaction mixture
  3. customto obtain a uniform solution

Sources & evidence

ORD record
ord-683c2b869e784110902240ea607a8698
Source dataset
uspto-grants-2013_10
Patent number
US08552182B2

Reaction notes

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