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Anisole → (4-Methoxyphenyl)(3-nitrophenyl)methanone

HRID 2230948
Notes
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Reaction equation

HRID 2230948 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][CH:12]=1)[C:7](Cl)=[O:8])([O-:3])=[O:2].[C:13]1([O:19][CH3:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[Cl-].[Al+3].[Cl-].[Cl-].C(OCC)(=O)C>ClCCl.O>[N+:1]([C:4]1[CH:5]=[C:6]([CH:10]=[CH:11][CH:12]=1)[C:7]([C:16]1[CH:17]=[CH:18][C:13]([O:19][CH3:20])=[CH:14][CH:15]=1)=[O:8])([O-:3])=[O:2]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 7519AnisoleHCID 8495Benzoyl chloride, 3-nitro-HCID 8857Ethyl AcetateHCID 6451240Aluminum(III) Chloride

Product 1

HCID 794540(4-Methoxyphenyl)(3-nitrophenyl)methanone

Reagents, catalysts & solvents 2

HCID 962WaterSolvent
HCID 6344DichloromethaneSolvent

Procedure

A mixture of 3-nitrobenzoyl chloride (3.71 g), anisole (2.0 ml) and aluminum chloride (2.67 g) in dichloromethane (50 ml) was refluxed for 1 hour. The reaction mixture was poured into a mixture of ethyl acetate and water. The organic phase was washed with brine, dried over magnesium sulfate and concentrated. The resultant solid was collected and washed with ethyl acetate to give 1-(3-nitrobenzoyl)-4-methoxybenzene (955 mg).

Workup

  1. temperaturewas refluxed for 1 hour
  2. washThe organic phase was washed with brine
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated
  5. customThe resultant solid was collected
  6. washwashed with ethyl acetate

Sources & evidence

ORD record
ord-b330f0dbe88e4848aa58c2cd13790b50
Source dataset
uspto-grants-2002_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06426345B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes