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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267965Generated: October 31, 2026

Sodium borohydride → HCID 23506277, compound

https://huagongshe.com/reaction/1267965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23506261HCID 23506261—
SolventMethanolHCID 887—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 23506277HCID 23506277—

Reaction Steps

2-(3-Acetylphenoxy)-3-[3-(pyridin-4-yl)propoxy]pyridine (0.20 g, 0.3 mmol) obtained in Example 60 is dissolved in methanol (10 ml), and thereto is added sodium borohydride (0.50 g, 13 mmol), and the mixture is stirred at room temperature for 10 minutes. To the reaction solution is added a saturated brine (50 ml), and the mixture is extracted with ethyl acetate (100 ml). The organic layer is washed with a saturated brine (50 ml×2), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: chloroform/methanol) to give 2-[3-(1-hydroxyethyl)phenoxy]-3-[3-(pyridin-4-yl)propoxy]pyridine, which is further treated with fumaric acid to give the title compound (0.06 g), m.p. 93-97° C. (recrystallized from ethanol/diethyl ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555557B1
Source datasetuspto-grants-2003_04
ORD IDord-a8dc9e4029994309a0c4ba66ff9d6c8e
Source noteuspto-grants-2003_04