N,N-Dimethylbenzamide → N,N-Dimethylbenzylamine

HRID 1588018Notes

Reaction equation

HRID 1588018 reaction equation
[CH3:1][N:2]([CH3:11])[C:3](=O)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C(O[SiH](OCC)OCC)C>CC(C)[O-].[Ti+4].CC(C)[O-].CC(C)[O-].CC(C)[O-].C1C=CC=CC=1>[CH3:1][N:2]([CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[CH3:11]

Participants

5

Conditions

Temperature
60 °C

Procedure

N,N-dimethylbenzamide (0.49 g, 3.0 mmol), triethoxysilane (1.4 mL, 7.5 mmol), titanium (IV) isopropoxide (0.04 mL, 0.15 mmol), and C6H6 (0.5 mL) were added to a flask open to the air and capped with a CaSO4 drying tube. The reaction mixture was heated to 60° C. for 16 hours. The solvent was removed in Vacuo and the contents were added to a mixture of 1 M NaOH (20mL) and THF (10mL). This mixture was stirred for 3 hours at room temperature and then poured into ethyl ether and washed with 1 M NaOH (5×50mL). The ether extracts were dried over MgSO4, filtered and the solvent was removed in vacuo to produce 0.30 g of N,N-dimethyl benzylamine as a yellowish oil (74% yield).

Workup

  1. customcapped with a CaSO4 drying tube
  2. customThe solvent was removed in Vacuo
  3. additionthe contents were added to a mixture of 1 M NaOH (20mL) and THF (10mL)
  4. additionpoured into ethyl ether
  5. washwashed with 1 M NaOH (5×50mL)
  6. dry with materialThe ether extracts were dried over MgSO4
  7. filtrationfiltered
  8. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-fbe591ed6c1c46cb9048fb72e708e34a
Source dataset
uspto-grants-1993_06
Patent number
US05220020

Reaction notes

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