N,N-Dimethylaniline → 3804-32-8

HRID 611446Notes

Reaction equation

HRID 611446 reaction equation
[N:1]([O-])=O.[Na+].[NH2:5][C:6]1[S:7][C:8]2[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=2[N:10]=1.S(=O)(=O)(O)O.[CH3:20][N:21]([CH3:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.C([O-])(=O)C.[Na+].[OH-].[Na+]>O>[CH3:20][N:21]([CH3:28])[C:22]1[CH:27]=[CH:26][C:25]([N:1]=[N:5][C:6]2[S:7][C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[N:10]=2)=[CH:24][CH:23]=1

Participants

8

Conditions

Temperature
0 °C

Procedure

An ice-cold solution of sodium nitrite (1.65 g, 23.9 mmol) in water (15 mL) was added slowly (via syringe) to a stirring mixture at 0° C. of 2-aminobenzothiazole (3.78 g, 25.2 mmol) in water (50 mL) and concentrated sulfuric acid (7.0 mL, 126.7 mmol). During addition, the temperature was kept below 5° C. The resultant orange mixture was stirred at 0° C. for 15 minutes, then N,N-dimethylaniline was added dropwise causing the mixture to turn dark brown-black. The mixture was stirred at 0° C. for 15 minutes, an aqueous solution of sodium acetate (4.32 g in 20 mL of water) was added dropwise, stirred for 1 hour, basified with 25% sodium hydroxide solution to a pH ~12 and allowed to warm to room temperature. The mixture was filtered, the solid was washed with cold water, recrystallized from methanol, then chromatographed (silica gel, 2% methanol in methylene chloride) to give the title compound as a green solid, mp 243-246° C.

Workup

  1. additionDuring addition
  2. customwas kept below 5° C
  3. stirringThe mixture was stirred at 0° C. for 15 minutes
  4. stirringstirred for 1 hour
  5. temperatureto warm to room temperature
  6. filtrationThe mixture was filtered
  7. washthe solid was washed with cold water
  8. customrecrystallized from methanol
  9. customchromatographed (silica gel, 2% methanol in methylene chloride)

Sources & evidence

ORD record
ord-00166c04a6524df2b4ae4627045d63bc
Source dataset
uspto-grants-1999_12
Patent number
US06001331

Reaction notes

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