Carbon Dioxide → 2-Tert-butyl-5-nitroaniline

HRID 2212692Notes

Reaction equation

HRID 2212692 reaction equation
OS(O)(=O)=O.C(=O)=O.[C:9]([C:13]1[CH:19]=[CH:18][CH:17]=[CH:16][C:14]=1[NH2:15])([CH3:12])([CH3:11])[CH3:10].[N+:20]([O-])([O-:22])=[O:21].[K+]>>[C:9]([C:13]1[CH:19]=[CH:18][C:17]([N+:20]([O-:22])=[O:21])=[CH:16][C:14]=1[NH2:15])([CH3:12])([CH3:10])[CH3:11]

Participants

5

Procedure

Concentrated H2SO4 (1 L) was cooled to −10° C. with a dry ice IpOH bath in a 2 L 3-neck round bottom flask fitted with a mechanical stirrer and temperature probe. 2-t-Butylaniline (109 g, 730 mmol) was added, giving a clumpy solid. Once the temperature of the mixture was stabilized at −10° C., KNO3 (101 g, 1001 mmol) was added portion-wise, as the solid, over 4 h, maintaining the temperature between −20 and −5° C. Once all of the KNO3 was added, the reaction was stirred overnight with gradual warming to RT. The reaction was quenched by diluting with H2O and extracting 3× with EtOAc. The EtOAc extracts were washed multiple times with saturated NaHCO3 (aq), until gas evolution ceased, then with brine. The EtOAc extracts were combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure giving a black oil. The oil was eluted through a 36×7 cm column of silica gel with a 5%; 10%; 15%; 25%; and 50% EtOAc:Hexanes step gradient (2 L each step) giving 2-tert-butyl-5-nitro-phenylamine as a red solid.

Workup

  1. customfitted with a mechanical stirrer
  2. customgiving a clumpy solid
  3. customwas stabilized at −10° C.
  4. temperaturemaintaining the temperature between −20 and −5° C
  5. customThe reaction was quenched
  6. additionby diluting with H2O
  7. extractionextracting 3× with EtOAc
  8. washThe EtOAc extracts were washed multiple times with saturated NaHCO3 (aq)
  9. dry with materialdried over anhydrous Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure
  12. customgiving a black oil
  13. washThe oil was eluted through a 36×7 cm column of silica gel with a 5%

Sources & evidence

ORD record
ord-d456e8b74df04412b9fa30a6362cffa0
Source dataset
uspto-grants-2006_09
Patent number
US07102009B2

Reaction notes

Loading…