Benzaldehyde → (+)-Benzylphenethylamine

To a stirred solution of benzaldehyde (1.58 mL, 15.5 mmol) in 10 mL of absolute ethanol at room temperature under nitrogen was added (R)-α-methylbenzylamine (2.0 mL, 15.51 mmol, 99% ee.). The reaction mixture was stirred for 3 hours. The reaction solution was then dried over magnesium sulfate and diluted to a 60 mL volume with EtOH. Ethanol washed Raney-Ni (~ 1.5 g) was added and the resulting suspension was treated with 58 psi of H2 in a Parr Type Shaker. After 1 day, additional Raney-Ni (~ 1 g) and 30 mL of ethanol were added and the hydrogenolysis continued for 3 days. The reaction mixture was filtered through. Celite to remove the catalyst and concentrated to afford 3.11 g (95%) of N-benzyl (R)-α-methylbenzylamine as a pale yellow oil contaminated with ~ 5% of benzyl alcohol and (R)-α-methylbenzylamine; 1H NMR (DMSO-d6, 250 MHz) δ 7.1-7.5 (m, 10 H, Ar), 3.68 (q, 1 H, J=6.6 Hz), 3.48 (dd, 2 H, J1 =13.6 Hz, J2 =20.5 Hz), 1.26 (d, 3 H, J=6.6 Hz, CH3); 13C NMR (DMSO-d6) δ 146.1, 141.0, 128.2, 128.0, 127.8, 126.5, 126.4, 56.7, 50.6, 24.5. This mixture was used directly in the next reaction.

1. dry with materialThe reaction solution was then dried over magnesium sulfate
2. additiondiluted to a 60 mL volume with EtOH
3. additionEthanol washed Raney-Ni (~ 1.5 g) was added
4. additionthe resulting suspension was treated with 58 psi of H2 in a Parr Type Shaker
5. waitAfter 1 day
6. additionadditional Raney-Ni (~ 1 g) and 30 mL of ethanol were added
7. waitthe hydrogenolysis continued for 3 days
8. filtrationThe reaction mixture was filtered through
9. customCelite to remove the catalyst
10. concentrationconcentrated

ORD record

ord-f13d57786ecf4054aaa7e0537f0a7109

Source dataset

uspto-grants-1997_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05605914