HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → HCID 86605369, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (2S)-2-butyloxirane | HCID 1549991 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86605369 | HCID 86605369 | 85% |
Reaction Steps
In a 50 mL-volumetric autoclave were added deaerated ethanol (10 mL) and ethyl acetate (10 mL), and thereto were added 4-aminopyridine (47 mg, 0.5 mmol) and (S)-1,2-epoxyhexane (2.0 g, 20 mmol, >99% ee). Then to the mixture was added crystalline dicobaltoctacarbonyl complex (171 mg, 0.5 mmol). After covering the autoclave with a cap, carbon monoxide (1 MPa) and hydrogen gas (1 MPa) were introduced therein and the mixture was reacted at 35° C. for 28 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (S)-3-hydroxyheptanoic acid ethyl ester (2.92 g, 85%, >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-ae50dea6e51241bc8778130daca9d8e9 |
| Source note | uspto-grants-2007_08 |