反应 #1121749

ord-cdc73814ccc542d68db084df397b1100

反应方程式

[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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他After 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
    其他The layers were separated
  4. 4
    萃取the aqueous layer was extracted once more with 10 mL of ethyl acetate
  5. 5
    浓缩Then the aqueous layer was concentrated

实验过程

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%.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08546112B2uspto-grants-2013_10