反应 #40272

反应方程式

2-isobutyl-succinonitrile

KOH

water

→

potassium (S)-3-cyano-5-methylhexanoate

收率 31.3%

反应条件

后处理

1. 1
   其他reaction vessels
2. 2
   其他the product mixtures were decanted
3. 3
   其他leaving the enzyme catalyst
4. 4
   其他in the reaction vessels
5. 5
   其他Reaction buffer (20 mL)
6. 6
   workup.ADDITIONwas added to the each reaction vessel
7. 7
   workup.STIRRINGstirred for approximately 2 min.
8. 8
   其他decanted
9. 9
   workup.ADDITIONadded to the product mixtures
10. 10
    workup.ADDITIONby adding
11. 11
    其他2-isobutyl-succinonitrile (6.81 g) and reaction buffer (118.2 mL) to each reaction vessel
12. 12
    workup.STIRRINGstirring the reaction
13. 13
    workup.WAITmixtures for 24 h
14. 14
    其他After four reactions were completed in each vessel
15. 15
    萃取extracted with MTBE (3×500 mL)
16. 16
    其他The MTBE extracts were removed
17. 17
    萃取extracted with MTBE (2×500 mL)
18. 18
    萃取The MTBE extract of the acidified aqueous part
19. 19
    浓缩was concentrated under vacuum
20. 20
    其他to leave an oil, which
21. 21
    浓缩The resulting solution was concentrated under vacuum

实验过程

Two 125 mL jacketed reaction vessels maintained at 30° C. were each charged with 2-isobutyl-succinonitrile (6.81 g), NIT-102 C2 (1.70 g) and 118.2 mL of reaction buffer. After stirring for 24 h, the product mixtures were decanted, leaving the enzyme catalyst in the reaction vessels. Reaction buffer (20 mL) was added to the each reaction vessel, stirred for approximately 2 min., and then decanted and added to the product mixtures. Reactions were repeated by adding 2-isobutyl-succinonitrile (6.81 g) and reaction buffer (118.2 mL) to each reaction vessel and stirring the reaction mixtures for 24 h. After four reactions were completed in each vessel (total of eight batch reactions), the product mixtures were combined and extracted with MTBE (3×500 mL). The MTBE extracts were removed and the aqueous part adjusted to pH 2.1 with phosphoric acid and extracted with MTBE (2×500 mL). The MTBE extract of the acidified aqueous part was concentrated under vacuum to leave an oil, which was treated with water (100 mL) and KOH (8.5 g). The resulting solution was concentrated under vacuum to give 24.2 g (31.3%) of potassium (S)-3-cyano-5-methylhexanoate. Methyl (S)-3-cyano-5-methylhexanoate was prepared from potassium (S)-3-cyano-5-methylhexanoate and analyzed by chiral GC to reveal an enantiomeric purity of 99.1% e.e.

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