Sodium Hydroxide → HCID 86743839, compound

HRID 2072732Notes

Reaction equation

HRID 2072732 reaction equation
[CH3:1][N:2]([CH3:24])[C:3]1[N:7]=[C:6]([CH:8]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16](=O)[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:11]=2)[CH3:9])[O:5][N:4]=1.Cl.[NH2:26][OH:27].[OH-].[Na+]>C(O)C.O>[CH3:1][N:2]([CH3:24])[C:3]1[N:7]=[C:6]([CH:8]([C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([C:16](=[N:26][OH:27])[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:11]=2)[CH3:9])[O:5][N:4]=1

Participants

6

Reactant 3

HCID 14798Sodium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 15676082HCID 15676082, compound

Product 1

HCID 86743839HCID 86743839, compoundYield 84%

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent2×

Procedure

To 3-dimethylamino-5-(1-(3-benzoylphenyl)ethyl)-1,2,4-oxadiazole (1.0 g, 3.11 mmol) in ethanol (10 ml) were added hydroxylamine hydrochloride (0.25 g, 3.45 mmol) in water (2 ml) and sodium hydroxide (0.40 g, 9.5 mmol) in water (2 ml). After reflux with stirring for 24 h, the mixture was poured upon ice water and extracted with ethyl acetate. The ethyl acetate extracts were washed with saturated NaCl aq. dried with anhydrous magnesium salfate, and evaporated under redused pressure to a residue, which was chromatographed to afford 3-dimethylamino-5-(1-(3-(α-hydroxyiminobenzyl)phenyl)ethyl)-1,2,4-oxadiazole (0.873 g, 84% yield) as oily substance: NMR(CDCl3)δ 1.66(d)+1.77(d) (3H), 2.98(s, 6H), 4.20(m, 1H), 7.22-7.55(m, 9H) ppm; IR(neat) 3700-3100, 1600, 1405 cm-1.

Workup

  1. temperatureAfter reflux
  2. extractionextracted with ethyl acetate
  3. washThe ethyl acetate extracts were washed with saturated NaCl aq.
  4. dry with materialdried with anhydrous magnesium salfate
  5. customevaporated under redused pressure to a residue, which
  6. customwas chromatographed

Sources & evidence

ORD record
ord-ffe58eb6962c44b9bc3e301d18e93f82
Source dataset
uspto-grants-1990_04
Patent number
US04914112

Reaction notes

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