Sodium Carbonate → HCID 14801185, compound

HRID 1682139Notes

Reaction equation

HRID 1682139 reaction equation
[CH3:1][O:2][CH2:3][C:4]1[C:5]([CH3:11])=[C:6]([CH:8]=[CH:9][CH:10]=1)[NH2:7].[S-:12][C:13]#[N:14].[Na+].[Br-].[Na+].BrBr.C(=O)([O-])[O-].[Na+].[Na+]>CO.C(Cl)(Cl)Cl.O>[CH3:1][O:2][CH2:3][C:4]1[C:5]([CH3:11])=[C:6]([CH:8]=[CH:9][C:10]=1[S:12][C:13]#[N:14])[NH2:7]

Participants

9

Conditions

Temperature
0 °C

Procedure

22.6 g (0.15 mol) of 3-methoxymethyl-2-methylaniline was dissolved in 300 ml of methanol. Then, 36.5 g of sodium thiocyanate was added thereto to obtain a uniform solution. This solution was cooled to 0° C., and 100 ml of a saturated methanol solution of sodium bromide with 25.2 g of bromine was dropwise added thereto so that the reaction temperature did not exceed 5° C. After the dropwise addition, the mixture was stirred at a temperature of not higher than 5° C. for 1 hour and at room temperature for 1 hour to complete the reaction. The reaction solution was poured into 1 liter of water and neutralized with a 5% sodium carbonate aqueous solution. Chloroform was added to extract the oily substance. The chloroform layer was washed with water and a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure to obtain 29.6 g of the desired product.

Workup

  1. customto obtain a uniform solution
  2. customdid not exceed 5° C
  3. additionAfter the dropwise addition
  4. waitat room temperature for 1 hour to complete
  5. customthe reaction
  6. extractionto extract the oily substance
  7. washThe chloroform layer was washed with water
  8. dry with materiala saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate
  9. distillationThen, the solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-a9100df0cfd24ac8ba013667e74981c1
Source dataset
uspto-grants-1992_12
Patent number
US05175299

Reaction notes

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