HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67777123, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67778223 | HCID 67778223 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67777123 | HCID 67777123 | 80.4% |
Reaction Steps
Sodium borohydride (0.109 g) was added to a solution of 2-[2-bromo-4-(cyclopropylmethoxy)phenyl]-1-(5-{[tris(1-methylethyl)silyl]oxy}pyridin-2-yl)ethanone (1.50 g) in ethanol (10 mL) at room temperature. The reaction mixture was stirred at room temperature for 1 hr, and the solvent was evaporated under reduced pressure. The residue was diluted with ethyl acetate and water, and the organic layer was separated. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.210 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08729102B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-7528aebe87cf427e91d2ac5eb4905963 |
| Source note | uspto-grants-2014_05 |