Sulfuric Acid → 1-Aminocyclohexanecarboxamide

HRID 2420199Notes

Reaction equation

HRID 2420199 reaction equation
S(=O)(=O)(O)O.[NH2:6][C:7]1([C:13]#[N:14])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1.[OH-:15].[Na+]>>[NH2:6][C:7]1([C:13]([NH2:14])=[O:15])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1

Participants

4

Conditions

Temperature
100 °C

Procedure

To 20 g concentrated sulfuric acid at 5° C is added with stirring 10 g of 1-aminocyclohexanecarbonitrile. After the addition, the mixture is heated with stirring at 100° C for 1 hour. The hot solution is then poured onto ice, the solution made strongly basic with 50% aqueous sodium hydroxide solution, and extracted three times with chloroform. The extract is washed with water, saturated NaHCO3 solution, dried, and the solvent removed in vacuo to leave the product, 1-aminocyclohexanecarboxamide, as a crystalline residue, melting point 99°-102° C. This can be recrystallized from either benzene or ether to give a pure product, melting point 101°-102° C.

Workup

  1. additionAfter the addition
  2. temperaturethe mixture is heated
  3. additionThe hot solution is then poured onto ice
  4. extractionextracted three times with chloroform
  5. washThe extract is washed with water, saturated NaHCO3 solution
  6. customdried
  7. customthe solvent removed in vacuo

Sources & evidence

ORD record
ord-10a4af5116874f8896889c3ec32836a0
Source dataset
uspto-grants-1978_08
Patent number
US04110103

Reaction notes

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