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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252332Generated: November 1, 2026

Sodium borohydride → HCID 17974485, compound

https://huagongshe.com/reaction/2252332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 17974502HCID 17974502—
SolventMethanolHCID 887—
ProductHCID 17974485HCID 17974485—

Reaction Steps

To a solution of 2-(6-chloro-pyridin-3-yloxy)-benzaldehyde (250 mg, 1.07 mmol) in methanol at ambient temperature was added sodium borohydride (49 mg, 1.3 mmol). The resulting reaction was stirred for 30 minutes, then quenched with saturated NaHCO3. The methanol was removed in vacuo, and the residue was diluted with water and extracted with ethyl acetate. The combined organics were washed with brine, dried over sodium sulfate, and concentrated in vacuo to an oil. The crude was purified by flash chromatography (eluting with 25% ethyl acetate/hexane) to give the above named compound as an oil (250 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07321040B2
Source datasetuspto-grants-2008_01
ORD IDord-85b4990ce9ea4d12a384763b2043b836
Source noteuspto-grants-2008_01