تفاعل #1121749

ord-cdc73814ccc542d68db084df397b1100

معادلة التفاعل

[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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter 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
    أخرىThe layers were separated
  4. 4
    استخلاصthe aqueous layer was extracted once more with 10 mL of ethyl acetate
  5. 5
    تركيزThen the aqueous layer was concentrated

الإجراء التجريبي

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%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08546112B2uspto-grants-2013_10