Acetanilide → HCID 9862611, compound

HRID 349403Notes

Reaction equation

HRID 349403 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)O)=[CH:4][CH:3]=1.[C:16]1([NH:22][C:23](=[O:25])[CH3:24])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>CC(O)=O.OS(O)(=O)=O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:10]2[CH:11]=[N:12][CH:13]=[CH:14][CH:15]=2)[C:19]2[CH:20]=[CH:21][C:16]([NH:22][C:23](=[O:25])[CH3:24])=[CH:17][CH:18]=2)=[CH:4][CH:3]=1

Participants

5

Reactant 2

HCID 904AcetanilideHCID 240724(4-chlorophenyl)(pyridin-3-yl)methanol

Product 1

HCID 9862611HCID 9862611, compoundYield 100%

Reagents, catalysts & solvents 2

HCID 176Acetic AcidSolventHCID 1118Sulfuric AcidSolvent

Procedure

A mixture of α-(4-chlorophenyl)-3-pyridinemethanol (0.364 mol) and N-phenyl acetamide (0.364 mol) in HOAc (360 ml) and H2SO4 36N (38.6 ml) was stirred and refluxed for 6 days. The solvent was evaporated, yielding 122.6 g (±)-N-[4-[(4-chlorophenyl)(3-pyridinyl)methyl]phenyl]acetamide (compound 673).

Workup

  1. temperaturerefluxed for 6 days
  2. customThe solvent was evaporated

Sources & evidence

ORD record
ord-3914a9b25a5b4b578c17ed5d6568a603
Source dataset
uspto-grants-2007_02
Patent number
US07179825B2

Reaction notes

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