HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → Ethyl (3R)-4-cyano-3-hydroxybutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ethyl (3S)-4-chloro-3-hydroxybutanoate | HCID 7019277 | — |
| Solvent | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Product | Ethyl (3R)-4-cyano-3-hydroxybutanoate | HCID 2733879 | — |
Reaction Steps
To a well stirred solution of ethyl (S)-4-chloro3-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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132267B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-df0bb5a321cd4ae0847a812b98d2085c |
| Source note | uspto-grants-2006_11 |