Reacción #75427

ord-a3c6958a412c4737b0184493e43e5a7a

Ecuación de reacción

[Na+].[OH-]
sodium hydroxide
Cl
hydrochloric acid
COC(=O)Cl
methyl chloroformate
N[C@H](Cc1ccccc1)C(=O)O
D-phenylalanine
[Na+].[OH-]
sodium hydroxide
COC(=O)N[C@H](Cc1ccccc1)C(=O)O
oil
Rendimiento 113.9%
COC(=O)N[C@H](Cc1ccccc1)C(=O)O
(R)-2-(Methoxycarbonylamino)-3-phenylpropanoic acid
Rendimiento 113.9%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONWhen the addition
  2. 2
    workup.ADDITIONwas also added dropwise
  3. 3
    ExtracciónThe acid was extracted twice with diethylether
  4. 4
    Lavadothe extracts were washed with brine
  5. 5
    Secadodried (MgSO4)
  6. 6
    OtroThe solvent was removed under vacuum

Procedimiento

A solution of D-phenylalanine (25.00 g, 0.151 mol) and sodium hydroxide (6.05 g, 0.151 mol) in water (170 ml) and tetrahydrofuran (225 ml) was cooled to −15° C., and a solution of methyl chloroformate (18.6 g, 0.197 mol) in tetrahydrofuran (50 ml) was added dropwise. When the addition was ˜half complete, a solution of sodium hydroxide (9.10 g, 0.227 mol) in water (20 ml) was also added dropwise. When the additions were complete, the mixture was stirred at room temperature for an additional 2 hours and acid fixed with 10% hydrochloric acid. The acid was extracted twice with diethylether, and the extracts were washed with brine and dried (MgSO4). The solvent was removed under vacuum to leave a clear oil (38.38 g). HPLC 6.01 min (78.9%), 7.32 min (5.0%), 8.29 min (10.8%), 8.42 min (0.5%), 9.95 min (1.2%), 10.27 min (2.8%), 11.92 min (0.7%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE038452E1uspto-grants-2004_03