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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841571Generated: November 2, 2026

Sodium borohydride → HCID 23506277, compound

https://huagongshe.com/reaction/1841571

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 numberUS06683186B2
Source datasetuspto-grants-2004_01
ORD IDord-2906368d31724aa29b5faa9b31c629dc
Source noteuspto-grants-2004_01