Reacción #1121749

ord-cdc73814ccc542d68db084df397b1100

Ecuación de reacción

[Na+].[OH-]
NaOH
[Na+].[OH-]
NaOH
CO
methanol
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
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 250 μL of methanol and 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 98%.

Fuente

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