HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854148Generated: October 31, 2026
Ethanol → Ethyl (3S)-4-chloro-3-hydroxybutanoate
https://huagongshe.com/reaction/854148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Product | Ethyl (3S)-4-chloro-3-hydroxybutanoate | HCID 7019277 | 92% |
Reaction Steps
In a 50 mL-volumetric autoclave were added deaerated ethanol (10 mL), and thereto were added cobalt acetate tetrahydrate (250 mg, 1 mmol) and 10% Pd/C (10 mg). After covering the autoclave with a cap, carbon monoxide (1 MPa) and hydrogen gas (1 MPa) were introduced therein, successively and the mixture was reacted at 80° C. for 3 hours. After 3 hours the mixture was cooled to room temperature, and the mixed gas was emitted to give a solution containing dicobaltoctacarbonyl complex. Thereto were added 4-aminopyridine (47 mg, 0.5 mmol) and (S)-epichlorohydrin (1.8 g, 20 mmol, >99% ee). After covering the autoclave with a cap, carbon monoxide (1 MPa) was introduced therein and the mixture was reacted at 35° C. for 28 hours. After temperature of the mixture was made room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-4-chloro-3- hydroxybutanoic acid ethyl ester (3.1 g, 92%, >99% ee) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256305B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-ce03cb5de30f4da7a7517cfa7311d7ef |
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| Source note | uspto-grants-2007_08 |
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