HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 11984349, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | (-)-Benzyl (R)-glycidyl ether | HCID 159746 | — |
| Reactant | HCID 178418416 | HCID 178418416 | — |
| Product | HCID 11984349 | HCID 11984349 | 95% |
Reaction Steps
In a 50 mL-volumetric autoclave were added deaerated methanol (10 mL) and t-butyl methyl ether (10 mL), and thereto were added 4-aminopyridine (47 mg, 0.5 mmol) and (R)-benzylglycidyl ether (3.3 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) was introduced therein and the mixture was reacted at 40° C. for 6 hours. After cooling to room temperature, the solvent was removed in vacuo. The residue was subjected to Kugelrohr distillation to give (R)-4-benzyloxy-3-hydroxybutanoic acid methyl ester (4.3 g, 95%, >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-a41df3f0fd4a4eff857533c76b29da7b |
| Source note | uspto-grants-2007_08 |