Reacción #1121748

ord-4e89febef8c74ebb971e131879a654bf

Ecuación de reacción

[Na+].[OH-]
NaOH
CCOC(=O)C[C@H](CC(C)C)C[N+](=O)[O-]
5-methyl-3-nitromethyl-hexanoic acid ethyl ester
CCOC(=O)C[C@H](CC(C)C)C[N+](=O)[O-]
(S)-5-methyl-3-nitromethyl-hexanoic acid ethyl ester
[Na+].[OH-]
NaOH
CC(C)C[C@@H](CC(=O)[O-])C[N+](=O)[O-].[Na+]
title compound
CC(C)C[C@@H](CC(=O)[O-])C[N+](=O)[O-].[Na+]
(S)-5-methyl-3-nitromethyl-hexanoic acid sodium salt

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroAfter 45% conversion (corresponding to 4.0 mL of 0.1M NaOH consumption) the reaction
  2. 2
    workup.ADDITIONwas stopped by addition of 10 mL of ethyl acetate
  3. 3
    OtroThe layers were separated
  4. 4
    Extracciónthe aqueous layer was extracted once more with 10 mL of ethyl acetate
  5. 5
    ConcentraciónThen the aqueous layer was concentrated

Procedimiento

In a beaker 100 mg of EstC (lyophilized) were dissolved/suspended in 10 mL of potassium phosphate buffer (1 mM, pH 7.2). The pH drops to pH ˜6.8 and was adjusted to pH=7.4 with aqueous NaOH (0.1 M). Then 200 mg of 5-methyl-3-nitromethyl-hexanoic acid ethyl ester (VIII, R1=ethyl) were added and the pH was kept at 7.4 by continuous addition of aqueous NaOH (0.1M). After 45% conversion (corresponding to 4.0 mL of 0.1M NaOH consumption) the reaction was stopped by addition of 10 mL of ethyl acetate. The layers were separated and the aqueous layer was extracted once more with 10 mL of ethyl acetate. Then the aqueous layer was concentrated to give the title compound with an ee of 88%.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08546112B2uspto-grants-2013_10