Hydrochloric Acid → HCID 11035364, compound

HRID 1938891Notes

Reaction equation

HRID 1938891 reaction equation
[C:1]1([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:6]=[CH:5][C:4]([O:7][CH2:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15](=[O:20])[C:16](OC)=[O:17])=[CH:3][CH:2]=1.C1COCC1.[CH3:32][NH2:33].Cl>CO.O>[CH3:32][NH:33][C:16](=[O:17])[C:15]([C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[CH2:8][O:7][C:4]1[CH:5]=[CH:6][C:1]([C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:2][CH:3]=1)=[O:20]

Participants

7

Procedure

To methyl 2-[2-(biphenyl-4-yloxymethyl)phenyl]-2-oxoacetate (3.46 g, 0.01 mol), added were anhydrous methanol (10 ml), dry THF (10 ml) and a 40% solution (2.33 g) of methyl amine (0.03 mol) in methanol, and the reaction mixture was stirred at room temperature for 2 hour. After completion of the reaction, water (150 ml) was added to the reaction mixture which was then adjusted to below PH 2 by addition of conc. HCl and extracted with ethyl acetate (150 ml). The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The obtained crystals (3.42 g; yield, 99.1%) were recrystallized from ethyl acetate/n-hexane to give N-methyl-2-[2-(biphenyl-4-yloxymethyl)phenyl]-2-oxoacetamide (2.83 g) as colorless crystals (m.p.: 144°-145° C.).

Workup

  1. additionwas added to the reaction mixture which
  2. extractionextracted with ethyl acetate (150 ml)
  3. dry with materialThe extract was dried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe obtained crystals (3.42 g; yield, 99.1%)
  6. customwere recrystallized from ethyl acetate/n-hexane

Sources & evidence

ORD record
ord-7feb620b55a1486a954b112df84cac58
Source dataset
uspto-grants-1997_12
Patent number
US05693859

Reaction notes

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