Potassium Hydroxide → 3-Chloro-4-methoxymethoxy-5-methylphenol

HRID 1420514Notes

Reaction equation

HRID 1420514 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([O:13]C(=O)C2C=CC=CC=2)[CH:5]=[C:6]([CH3:12])[C:7]=1[O:8][CH2:9][O:10][CH3:11].[OH-].[K+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([OH:13])[CH:5]=[C:6]([CH3:12])[C:7]=1[O:8][CH2:9][O:10][CH3:11]

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 185046333-Chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene

Product 1

HCID 185045733-Chloro-4-methoxymethoxy-5-methylphenolYield 101.3%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Then, 26 g of 3-chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene was dissolved in 200 ml of methanol, and the solution was stirred at room temperature for 1 hour, while adding dropwise 60 ml of 10% aqueous potassium hydroxide solution. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was added to 150 ml of water, neutralized with 10% aqueous hydrochloric acid solution, and extracted with 200 ml of diethyl ether. The solvent was removed by distillation under reduced pressure, and the residue was subjected to silica gel chromatography, which afforded 17.4 g of 3-chloro-4-methoxymethoxy-5-methylphenol (96% yield).

Workup

  1. customAfter completion of the reaction
  2. customthe solvent was removed by distillation under reduced pressure
  3. additionThe residue was added to 150 ml of water
  4. extractionextracted with 200 ml of diethyl ether
  5. customThe solvent was removed by distillation under reduced pressure

Sources & evidence

ORD record
ord-6303c2dd551349d097c3ba1e196d8bc9
Source dataset
uspto-grants-2000_06
Patent number
US06071861

Reaction notes

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