反应 #1121747

ord-0221fc97b51c4b36a2f8474f2ef57606

反应方程式

CCOC(=O)CC(CC(C)C)C[N+](=O)[O-]
5-methyl-3-nitromethyl-hexanoic acid ethyl ester
[Na+].[OH-]
NaOH
CCOC(=O)C[C@H](CC(C)C)C[N+](=O)[O-]
(S)-5-methyl-3-nitromethyl-hexanoic acid ethyl ester
收率 43.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他After 55% conversion (corresponds to 50.6 mL of NaOH consumption) the reaction
  2. 2
    workup.ADDITIONwas stopped by addition of 100 mL of ethyl acetate
  3. 3
    workup.ADDITION100 mL of 5M aqueous NaOH were added
  4. 4
    其他the layers were separated
  5. 5
    洗涤The aqueous layer was washed once with 100 mL of ethyl acetate
  6. 6
    浓缩The combined organic layers were concentrated under reduced pressure

实验过程

100 g of 5-methyl-3-nitromethyl-hexanoic acid ethyl ester (VIII, R1=ethyl) were added to an aqueous solution of EstB (500 mL cell extract; ˜5 g total protein concentration). At a temperature of 25° C. the pH was kept at 7.0 by continuous addition of 5M aqueous NaOH. After 55% conversion (corresponds to 50.6 mL of NaOH consumption) the reaction was stopped by addition of 100 mL of ethyl acetate. 100 mL of 5M aqueous NaOH were added and the layers were separated. The aqueous layer was washed once with 100 mL of ethyl acetate. The combined organic layers were concentrated under reduced pressure to give 43 g of (S)-5-methyl-3-nitromethyl-hexanoic acid ethyl ester (VIII, R1=ethyl; ee=98%).

来源

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