HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propyloxy]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(3-Phthalimidopropyloxy)pyridine | HCID 19079090 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-[3-(3-Hydroxyisoindolin-1-on-2-yl)propyloxy]pyridine | HCID 19079198 | 54.2% |
Reaction Steps
Sodium borohydride [1.89 g (50 mmol)] was added to a solution of 2.82 g (10.0 mmol) of 4-(3-phthalimidopropyloxy)pyridine in 150 ml of ethanol. The mixture was stirred at room temperature for 15 minutes. After the solvent was distilled off, brine was added to the residue. The mixture was extracted with chloroform and dried over anhydrous magnesium sulfate, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: ethanol/ethyl acetate=1:10), and then recrystallized from ethyl acetate to obtain 1.54 g of the desired compound (yield: 54.2%, colroless crystals).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246948 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-65c49a041cb1404cbaeaf61fdae85da3 |
| Source note | uspto-grants-1993_09 |