Potassium Bromide → HCID 12070506, compound

HRID 1636061Notes

Reaction equation

HRID 1636061 reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([C:11]2[CH:12]=[C:13]([N+:27]([O-:29])=[O:28])[CH:14]=[C:15]([C:17]([C:19]3[CH:24]=[CH:23][C:22]([O:25]C)=[CH:21][CH:20]=3)=[O:18])[CH:16]=2)=[O:10])=[CH:5][CH:4]=1.Cl.N1C=CC=CC=1.[K+].[Br-]>O>[OH:2][C:3]1[CH:4]=[CH:5][C:6]([C:9]([C:11]2[CH:12]=[C:13]([N+:27]([O-:29])=[O:28])[CH:14]=[C:15]([C:17](=[O:18])[C:19]3[CH:20]=[CH:21][C:22]([OH:25])=[CH:23][CH:24]=3)[CH:16]=2)=[O:10])=[CH:7][CH:8]=1

Participants

5

Reactant 3

HCID 253877Potassium BromideHCID 10176127Pyridinium chlorideHCID 120705053,5-bis(4-methoxyphenylcarbonyl)nitrobenzene

Product 1

HCID 12070506HCID 12070506, compoundYield 96%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
120 °C

Procedure

Into a 250 mL three-necked, round-bottomed flask equipped with a magnetic stirrer, a condenser, and nitrogen inlet, 3,5-bis(4-methoxyphenylcarbonyl)nitrobenzene (6.2 g, 15.8 mmol) and freshly prepared pyridine hydrochloride (100 g) were placed. The mixture was heated under reflux until the solution became homogeneous. It took about 4 h. After cooled down 120° C., the mixture was poured into water. The resulting precipitate was collected and dried. The yellow solid was slurred in boiling toluene and collected by suction filtration to give 5.5 g (96% yield), m.p. 230-231.8° C. Anal. Calcd. for C20H13NO6: C, 66.12%; H, 3.61%; N, 3.86%; O, 26.42%. Found: C, 66.07%; H, 3.64%; N, 3.67%; O, 17.01%. FT-IR (KBr, cm−1): 1321, 1538 (A-NO2), 1602, 1648 (carbonyl), 3420 (Ar-OH). Mass spectrum (m/e): 363 (M+, 100% relative abundance). 1H-NMR (DMSO-d6, δ in ppm): 6.93-6.96 (d, 4H, Ar), 7.76-7.79 (d, 4H, Ar), 8.23 (s 1H, Ar), 8.58 (s, 2H, Ar), 10.66 (s, 2H, OH). 13C-NMR (DMSO-d6, δ in ppm) 115.48, 126.02, 126.65, 132.84, 134.83, 139.44, 147.61, 156.80, 162.70, 191.36.

Workup

  1. customInto a 250 mL three-necked, round-bottomed flask equipped with a magnetic stirrer, a condenser, and nitrogen inlet
  2. temperatureThe mixture was heated
  3. temperatureunder reflux until the solution
  4. customThe resulting precipitate was collected
  5. customdried
  6. filtrationcollected by suction filtration
  7. customto give 5.5 g (96% yield), m.p. 230-231.8° C

Sources & evidence

ORD record
ord-51dd37a2749d4efeaabb2a9508909856
Source dataset
uspto-grants-2003_01
Patent number
US06512124B1

Reaction notes

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