HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854149Generated: October 31, 2026
4-Aminopyridine → HCID 11052254, compound
https://huagongshe.com/reaction/854149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (+)-Epichlorohydrin | HCID 149428 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Catalyst | Cobalt(II) acetate tetrahydrate | HCID 61372 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 11052254 | HCID 11052254 | 92% |
Reaction Steps
In a 50 mL-volumetric autoclave were added deaerated isopropanol (10 mL) and THF (10 mL), and thereto were added cobalt acetate tetrahydrate (250 mg, 1 mmol) and 10% Rh/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 100° 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 (1.3 MPa) was introduced therein and the mixture was reacted at 35° C. for 30 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-4-chloro-3-hydroxybutanoic acid isopropyl ester (3.3 g, 92%, >99% ee) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07256305B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-28fc7587e4a54ef09833bd79cb9189c0 |
|---|
| Source note | uspto-grants-2007_08 |
|---|