Hydrochloric Acid → HCID 12897331, compound

HRID 1730679Notes

Reaction equation

HRID 1730679 reaction equation
Cl.[Cl:2][C:3]1[C:10]([N+:11]([O-])=O)=[CH:9][C:8]([N+:14]([O-])=O)=[CH:7][C:4]=1[C:5]#[N:6].[OH-].[Na+]>>[Cl:2][C:3]1[C:10]([NH2:11])=[CH:9][C:8]([NH2:14])=[CH:7][C:4]=1[C:5]#[N:6]

Participants

4

Procedure

To a solution of 194 gm. (0.86 mole) of stannous chloride dihydrate in 475 ml. of concentrated hydrochloric acid is added 27.5 gm. (0.12 mole) of 2-chloro-3,5-dinitrobenzonitrile. The temperature rises to 84° and a solution occurs. The mixture is allowed to cool to room temperature, placed in an ice-bath, cooled to 0° and a cold 50% sodium hydroxide solution is added, with cooling, until the mixture is strongly basic. The gelatinous precipitate is removed by filtration. The precipitate is washed thoroughly (4 times) with portions of ethyl acetate. The combined ethyl acetate washes are used to extract the aqueous filtrate. The combined ethyl acetate extracts are dried over anhydrous MgSO4 and the solvent removed by distillation. The residue is recrystallized from ethanol. There is obtained 11.30 gm. (56%) of colorless needles melting at 181°-82°.

Workup

  1. customrises to 84°
  2. customplaced in an ice-bath
  3. temperaturecooled to 0°
  4. temperaturewith cooling, until the mixture
  5. customThe gelatinous precipitate is removed by filtration
  6. washThe precipitate is washed thoroughly (4 times) with portions of ethyl acetate
  7. extractionto extract the aqueous filtrate
  8. dry with materialThe combined ethyl acetate extracts are dried over anhydrous MgSO4
  9. customthe solvent removed by distillation
  10. customThe residue is recrystallized from ethanol
  11. customThere is obtained 11.30 gm

Sources & evidence

ORD record
ord-d3a0c0bbe8c54abca48cad2aea3430b0
Source dataset
uspto-grants-1976_11
Patent number
US03993679

Reaction notes

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