Réaction #1244289
ord-6c78e85283f6422ba2ca5be721cb5544
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1LavageAfter fifty seven hours the mixture was washed with ethyl acetate (2 times 250 mL)
- 2Séchagethe combined organics dried over anhydrous sodium sulfate
- 3FiltrationThe mixture was filtered
- 4Autreevaporated on a rotary evaporator
Mode opératoire
To a well stirred solution of ethyl (S)-4-chloro-3-hydroxybutyrate (8.25 g, 50 mmoles) in 300 mM potassium phosphate buffer, 300 mM NaCN pH 8.0 (1 L) at 30° C. was added halohydrin dehalogenase SEQ ID NO: 14 (9 g) as a lyophilized powder. After fifty seven hours the mixture was washed with ethyl acetate (2 times 250 mL) and the combined organics dried over anhydrous sodium sulfate. The mixture was filtered and evaporated on a rotary evaporator to give essentially pure ethyl (R)-4-cyano-3-hydroxybutyrate, as determined using the gas chromatography method and elution time data described in Example 6, hereinbelow.