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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026242Generated: November 3, 2026

Sodium borohydride → HCID 67777123, compound

https://huagongshe.com/reaction/1026242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 67778223HCID 67778223—
SolventEthanolHCID 702—
ProductHCID 67777123HCID 6777712380.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729102B2
Source datasetuspto-grants-2014_05
ORD IDord-7528aebe87cf427e91d2ac5eb4905963
Source noteuspto-grants-2014_05