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Hydrochloric Acid → 2-(Hydroxymethyl)-4-methoxyphenol

HRID 1081868
Notes
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Reaction equation

HRID 1081868 reaction equation
[CH3:1][O:2][C:3]1[CH:10]=[C:7]([CH:8]=[O:9])[C:6]([OH:11])=[CH:5][CH:4]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3].Cl>CCOCC>[OH:9][CH2:8][C:7]1[CH:10]=[C:3]([O:2][CH3:1])[CH:4]=[CH:5][C:6]=1[OH:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 956952-Hydroxy-5-methoxybenzaldehydeHCID 21226445Aluminium lithium hydride2×

Product 1

HCID 4802532-(Hydroxymethyl)-4-methoxyphenolYield 77%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent3×

Procedure

Under ice cooling, the solution of 5-methoxysalicylaldehyde (5 g) in ether (20 ml) was slowly added dropwise to the suspension of LiAlH4 (0.75 g) in ether (50 ml). After stirring at room temperature for 2 hours, another addition of LiAlH4 (0.5 g) was carried out under ice cooling, with subsequent stirring at room temperature for 30 minutes. To the reaction solution was added ice carefully, followed by sequential addition of 1N HCl and ether. After filtering off insoluble materials using Celite™, the ether layer was separated from the filtrate, and then, the aqueous phase was further extracted with ether. The combined ether layers were washed with saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was washed with ether-hexane and filtered to give the title compound (3.9 g; 77%).

Workup

  1. stirringwith subsequent stirring at room temperature for 30 minutes
  2. additionTo the reaction solution was added ice carefully
  3. filtrationAfter filtering off insoluble materials
  4. customthe ether layer was separated from the filtrate
  5. extractionthe aqueous phase was further extracted with ether
  6. washThe combined ether layers were washed with saturated sodium chloride solution
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent was removed under reduced pressure
  9. washthe residue was washed with ether-hexane
  10. filtrationfiltered

Sources & evidence

ORD record
ord-3fd9f54b074d4167a284ff76df634988
Source dataset
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05587392

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes