반응 #440434

ord-c56e3c6712584ea59046da4379673638

반응 방정식

N[C@H](CO)C(=O)O
D-serine
[BH3-]C#N.[Na+]
sodium cyanoborohydride
O=Cc1ccccc1
benzaldehyde
O=C(O)[C@@H](CO)NCc1ccccc1
desired compound
수율 60.0%
O=C(O)[C@@H](CO)NCc1ccccc1
N-Benzyl-D-serine
수율 60.0%

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타at 30° C
  2. 2
    기타at room temperature
  3. 3
    여과Then, the mixture was filtered
  4. 4
    세척rinsed with methanol (50 mL)
  5. 5
    기타The white solid was dried in a vacuum oven at 40° C.
  6. 6
    workup.WAIT10 mmHg over 2 nights
  7. 7
    기타the solvent was evaporated

실험 절차

To a mixture of D-serine (25.0 g, 0.237 mol) and 200 mL anhydrous methanol was added sodium cyanoborohydride (11.95 g, 0.190 mol), while maintaining the temperature at 0° C. with an ice bath. Then, benzaldehyde (26.5 mL, 0.261 mol) was added to the reaction flask, dropwise, at 30° C. The mixture was stirred for 60 Hr. at room temperature. Then, the mixture was filtered and rinsed with methanol (50 mL). The white solid was dried in a vacuum oven at 40° C. and 10 mmHg over 2 nights: 24.5 g. The filtrate was retained and the solvent was evaporated. This oil was passed through a silica gel column (10% MeOH/CH2Cl2) and 3.4 g of the desired compound was isolated. The total amount of the product was 27.9 g (60.0% yield). 1H NMR (DMSO-d6) δ3.25 (m, 1H, CH), 3.85 (m, 2H, CH2), 4.11 (d, 2H, benzylic CH2), 7.45-7.53 (m, 5H, ArH).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06750216B2uspto-grants-2004_06