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M-Cresol → 3-(3-Methylphenoxy)benzaldehyde

HRID 2422252
Notes
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Reaction equation

HRID 2422252 reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[CH:10]1[C:15]([OH:16])=[CH:14][CH:13]=[CH:12][C:11]=1[CH3:17].C(=O)([O-])[O-].[K+].[K+].N1C2C(=CC=CC=2)C=CC=1>[Cu]=O.N1C=CC=CC=1>[CH3:17][C:11]1[CH:10]=[C:15]([CH:14]=[CH:13][CH:12]=1)[O:16][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 342M-CresolHCID 7047QuinolineHCID 11430Potassium CarbonateHCID 765833-Bromobenzaldehyde

Product 1

HCID 230829033-(3-Methylphenoxy)benzaldehydeYield 72.1%

Reagents, catalysts & solvents 2

HCID 14829Copper oxide
Catalyst
HCID 1049PyridineSolvent

Conditions

Temperature
170 °C

Procedure

A mixture of 3-bromobenzaldehyde (7.01 g, 37.9 mmol), m-cresol (4.51 g, 41.7 mmol), copper oxide (II) (4.53 g, 56.9 mmol), potassium carbonate (7.86 g, 56.9 mmol), pyridine (50 mL) and quinoline (25 mL) was stirred under a nitrogen atmosphere at 170° C. for 24 hrs. The reaction mixture was cooled and pyridine was evaporated under reduced pressure. Ethyl acetate was added to the residue, the insoluble material was filtered off, and the filtrate was washed with 1 M hydrochloric acid and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (hexane-10% ethyl acetate/hexane) to give the title compound (5.80 g, 72%) as a pale-brown oil.

Workup

  1. temperatureThe reaction mixture was cooled
  2. custompyridine was evaporated under reduced pressure
  3. additionEthyl acetate was added to the residue
  4. filtrationthe insoluble material was filtered off
  5. washthe filtrate was washed with 1 M hydrochloric acid and saturated brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe solvent was evaporated under reduced pressure
  8. customthe residue was purified by silica gel column chromatography (hexane-10% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-83e5591d14fe4cd6aa276420a9bd8bc1
Source dataset
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07960369B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes