Sulfuric Acid → HCID 14281515, compound

HRID 980537Notes

Reaction equation

HRID 980537 reaction equation
[CH:1]([C:4]([CH3:14])([N:7]1[C:11](=[O:12])[CH:10]=[CH:9][C:8]1=[O:13])[C:5]#[N:6])([CH3:3])[CH3:2].S(=O)(=O)(O)[OH:16].[Cl-].[Na+].C(OCC)(=O)C>C(Cl)Cl>[CH:1]([C:4]([CH3:14])([N:7]1[C:11](=[O:12])[CH:10]=[CH:9][C:8]1=[O:13])[C:5]([NH2:6])=[O:16])([CH3:3])[CH3:2]

Participants

6

Procedure

A solution of α-isopropyl-α-methyl-2,5-dioxo-3-pyrroline-1-acetonitrile (2.0 g, 0.104 mol) in methylene chloride (30 ml) is added in a fine stream to concentrated sulfuric acid at room temperature. After stirring overnight at room temperature for 16 hours the mixture is poured onto ice, containing sodium chloride and ethyl acetate. The organic layer is washed with aqueous sodium bicarbonate, brine and dried. Evaporation after washing with ether-pentane gives a solid (72%), mp 138.5°-140° C. Anal. calcd. for C10H14N2O3 : C, 57.13; H, 6.71; N, 13.33. Found: C, 56.89; H, 6.64; N, 13.16.

Workup

  1. additionis poured onto ice
  2. washThe organic layer is washed with aqueous sodium bicarbonate, brine
  3. customdried
  4. customEvaporation
  5. washafter washing with ether-pentane

Sources & evidence

ORD record
ord-04819e4978924770acc47a2caba76459
Source dataset
uspto-grants-1987_01
Patent number
US04638068

Reaction notes

Loading…