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Propofol → 2,6-Diisopropylanisole

HRID 1978550
Notes
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Reaction equation

HRID 1978550 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[OH:13])([CH3:3])[CH3:2].[C:14](=O)([O-])[O-].[K+].[K+].CI>CC(C)=O>[CH:10]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:5]=1[O:13][CH3:14])([CH3:12])[CH3:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 4943PropofolHCID 6328Methyl iodideHCID 11430Potassium Carbonate

Product 1

HCID 6009752,6-DiisopropylanisoleYield 72.7%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

A mixture of 2,6-diisopropyl phenol (20 g, 0.11 mol), potassium carbonate (62 g, 0.45 mol), acetone (160 ml) and methyl iodide (28 ml, 0.45 mole) is refluxed for three days. The reaction mixture is filtered through celite, evaporated, dissolved in ether, washed twice with 1M sodium hydroxide, dried over magnesium sulphate and concentrated to afford 15.1 g (0.08 mol, 70%) of 2,6-diisopropyl anisole as a slightly yellow oil.

Workup

  1. temperatureis refluxed for three days
  2. filtrationThe reaction mixture is filtered through celite
  3. customevaporated
  4. dissolutiondissolved in ether
  5. washwashed twice with 1M sodium hydroxide
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-411693b5b3764535bc789d07b141db72
Source dataset
uspto-grants-2001_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06236946B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes