반응 #11013

ord-96950af56707463597c262dab0ced699

반응 방정식

O=N[O-].[Na+]
sodium nitrite
N[C@@H](Cc1ccccc1)C(=O)O
L-phenylalanine
O=C(O)[C@@H](O)Cc1ccccc1
(2S)-2-hydroxy-3-phenylpropionic acid
수율 85.0%

시약

없음

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출After extraction with three 100-ml portions of ethyl acetate
  2. 2
    건조the organic phase was dried over sodium sulfate
  3. 3
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

실험 절차

A solution of 14 g (217 mmol) of sodium nitrite in 20 ml of water was added dropwise to a solution of 14 g (85 mmol) of L-phenylalanine in 100 ml of 1 N sulfuric acid at 0° C. over 3 hours, and the mixture was stirred overnight at room temperature. After extraction with three 100-ml portions of ethyl acetate, the organic phase was dried over sodium sulfate. The optical purity of (2S)-2-hydroxy-3-phenylpropionic acid in this extract was 93.0% ee. The solvent was distilled off under reduced pressure to give 12 g of crude (2S)-2-hydroxy-3-phenylpropionic acid. Further, this crude product was purified by recrystallization using 35 ml of ethyl acetate to give 7.5 g (yield 53%) of the desired (2S)-2-hydroxy-3-phenylpropionic acid. The proton concentration (normality) in the reaction of this comparative example was 1.0 mol/kg, the amount of the protonic acid was 1.2 equivalents (relative to L-phenylalanine), and the reaction temperature was 0° C. to room temperature.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07094926B2uspto-grants-2006_08