HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610633Generated: October 26, 2026
Ethyl Acetate → Ethyl (3R)-4-cyano-3-hydroxybutanoate
https://huagongshe.com/reaction/610633
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ethyl (R)-(+)-4-bromo-3-hydroxybutyrate | HCID 12408095 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl (3R)-4-cyano-3-hydroxybutanoate | HCID 2733879 | 59.8% |
Reaction Steps
To a 50 gallon reactor containing a solution of 2.2 kg (44 mol) of sodium cyanide dissolved in 40 L of demineralized water was added 7 kg (33 mol) of (S)-4-bromo-3-hydroxybutyric acid, ethyl ester (Example 3) dissolved in 8 L of ethanol. The reaction mixture was stirred for 16 hours at room temperature. Ethyl acetate (65 L) was added, the mixture agitated, and the layers were allowed to separate. The lower aqueous layer was transferred to a 50 gallon vessel containing 2.5 kg of sodium chloride and 65 L of ethyl acetate, the mixture was agitated and the layers allowed to separate, and the lower aqueous layer was cut off. The organic layers were combined and concentrated in vacuo. The residue was distilled to afford 3.1 kg of the title compound; bp 110-125° C. 0.5 mm Hg; optical rotation [α]D25 =33.1° (C=1.08, chloroform);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998633 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-a5e5910e00c0485582a652197f61f684 |
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| Source note | uspto-grants-1999_12 |
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