Water → 4-(Aminomethyl)benzonitrile

HRID 1067987Notes

Reaction equation

HRID 1067987 reaction equation
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[N:20]([CH2:23][C:24]1[CH:31]=[CH:30][C:27]([C:28]#[N:29])=[CH:26][CH:25]=1)=[N+]=[N-].O>C1COCC1.CCOCC>[NH2:29][CH2:28][C:27]1[CH:30]=[CH:31][C:24]([C:23]#[N:20])=[CH:25][CH:26]=1

Participants

6

Procedure

Triphenylphosphine (7.67 g) is added to a solution of 4-(azidomethyl)-benzonitrile (4.19 g) in THF (30 mL) and stirred for 1 hr. Water (10 mL) is added, and the solution is stiffed for 16 hrs. The reaction mixture is diluted with ether (50 mL) and extracted with HCl (3 N, 3×25 mL) and water (1×25 mL). The aqueous phases are combined and washed with ether (50 mL). Sodium hydroxide is added until the pH=12. After extracting with ether (2×50 mL), the solution is dried with MgSO4 and filtered. The solvent is evaporated under reduced pressure. The resulting crude mixture is then purified via bulb to bulb distillation at 150° C. and 1 torr to afford 1.74 g (50%) of the title compound as a clear, colorless oil.

Workup

  1. waitthe solution is stiffed for 16 hrs
  2. extractionextracted with HCl (3 N, 3×25 mL) and water (1×25 mL)
  3. washwashed with ether (50 mL)
  4. additionSodium hydroxide is added until the pH=12
  5. extractionAfter extracting with ether (2×50 mL)
  6. dry with materialthe solution is dried with MgSO4
  7. filtrationfiltered
  8. customThe solvent is evaporated under reduced pressure
  9. distillationThe resulting crude mixture is then purified via bulb to bulb distillation at 150° C.

Sources & evidence

ORD record
ord-e81610b6db00485f9ae592a6aa162004
Source dataset
uspto-grants-2001_06
Patent number
US06248739B1

Reaction notes

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