Nitric Acid → HCID 178468310, compound

HRID 1895185Notes

Reaction equation

HRID 1895185 reaction equation
[CH3:1][CH:2]([C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH2:6])[CH3:3].P(=O)(O)(O)O.[N+]([O-])(O)=O.[N:20]([O-])=O.[Na+].C([O-])(=O)C.[K+].[C:29]([CH2:32][C:33](=[O:35])[CH3:34])(=[O:31])[CH3:30]>O.C(O)C>[CH3:1][CH:2]([C:4]1[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=1[NH:6][N:20]=[C:32]([C:33](=[O:35])[CH3:34])[C:29](=[O:31])[CH3:30])[CH3:3]

Participants

9

Conditions

Temperature
0 °C

Procedure

2-(1-Methylethyl)aniline (2.00 g, 14.81 mmol) was added to a solution of 12 mL of phosphoric acid (85%) and 8 mL of nitric acid (65%) at −6° C., followed by sodium nitrite (1.23 g, 17.78 mmol) in 4 mL of water dropwise at 0° C., and the mixture was stirred at 0° C. for 30 min. Then, to the reaction mixture was added dropwise a solution of potassium acetate (4.35 g, 44.43 mmol) and acetylacetone (1.92 g, 19.25 mmol) in 80 mL of ethanol and 20 mL of water. The mixture was stirred at room temperature overnight, filtered, washed with water, EtOH/H2O (1/1) and hexane, and dried to give the title compound (0.98 g, 27% yield): 1H NMR (400 MHz, CDCl3): δ ppm 1.34 (6H, d, J=6.8 Hz), 2.52 (3H, s), 2.63 (3H, s), 3.12-3.21 (1H, m), 7.19-7.23 (1H, m), 7.28-7.34 (2H, m), 7.77-8.00 (1H, m), 15.23 (1H, brs).

Workup

  1. stirringThe mixture was stirred at room temperature overnight
  2. filtrationfiltered
  3. washwashed with water, EtOH/H2O (1/1) and hexane
  4. customdried

Sources & evidence

ORD record
ord-98fb2b7dd33e4f23860da5ad1b9873eb
Source dataset
uspto-grants-2013_08
Patent number
US08513251B2

Reaction notes

Loading…