Dimethylamine → N,N-dimethyl-3-nitrobenzamide

HRID 864559Notes

Reaction equation

HRID 864559 reaction equation
[CH3:1][NH:2][CH3:3].[N+:4]([C:7]1[CH:8]=[C:9]([CH:13]=[CH:14][CH:15]=1)[C:10](Cl)=[O:11])([O-:6])=[O:5].C(OCC)(=O)C>O1CCOCC1>[CH3:1][N:2]([CH3:3])[C:10](=[O:11])[C:9]1[CH:13]=[CH:14][CH:15]=[C:7]([N+:4]([O-:6])=[O:5])[CH:8]=1

Participants

5

Reactant 3

HCID 674DimethylamineHCID 8495Benzoyl chloride, 3-nitro-HCID 8857Ethyl Acetate

Product 1

HCID 347759N,N-dimethyl-3-nitrobenzamide

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Procedure

Dimethylamine (50% aqueous solution, 3.6 ml) was stirred in an ice bath and a solution of 3-nitrobenzoyl chloride (1.8 g) in 1,4-dioxan (4 ml) was dropwise added thereto. The resulting mixture was stirred vigorously at ambient temperature for 2.5 hours. Ethyl acetate was added and organic layer was washed with water, 1N hydrochloric acid, 1N sodium hydroxide, water and saturated sodium chloride solution successively and dried over anhydrous magnesium sulfate. After filtration and concentration, the residue was recrystallized from benzene-n-hexane to afford N,N-dimethyl-3-nitrobenzamide (1.5 g) as a pale yellow prism.

Workup

  1. washorganic layer was washed with water, 1N hydrochloric acid, 1N sodium hydroxide, water and saturated sodium chloride solution successively
  2. dry with materialdried over anhydrous magnesium sulfate
  3. filtrationAfter filtration and concentration
  4. customthe residue was recrystallized from benzene-n-hexane

Sources & evidence

ORD record
ord-a623bc856ed54e94a271ab65e1c14b6d
Source dataset
uspto-grants-1996_10
Patent number
US05563162

Reaction notes

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