HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 59075095, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59075084 | HCID 59075084 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59075095 | HCID 59075095 | 85.4% |
Reaction Steps
To a solution of 7-{(R)-2-[(E)-3-(3-bromo-phenyl)-3-oxo-propenyl]-5-oxo-pyrrolidin-1-yl}-heptanoic acid methyl ester (0.78 g, 1.79 mmol) in 15 mL of methanol stirred at 0° C. under nitrogen was added sodium borohydride (0.074 g). The reaction mixture was stirred at room temperature for 6 hours. After addition of 1 N HCl solution the mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, concentrated, and purified by chromatography eluting with 50% EtOAc and Hexane followed by 100% EtOAc to yield 670 mg of 7-{(R)-2-[(E)-3-(3-bromo-phenyl)-3-hydroxy-propenyl]-5-oxo-pyrrolidin-1-yl}-heptanoic acid methyl ester. Step 3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900336B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-9c80e33cfd324e49bd5c73872addd0bc |
| Source note | uspto-grants-2005_05 |