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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392670Generated: October 26, 2026

Sodium borohydride → (2,6-Dichloro-3-hydroxymethyl-pyridin-4-yl)-pyrrolidin-1-yl-methanone

https://huagongshe.com/reaction/1392670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2,6-Dichloro-4-(pyrrolidine-1-carbonyl)-pyridine-3-carbaldehydeHCID 86593985—
SolventEthanolHCID 702—
Product(2,6-Dichloro-3-hydroxymethyl-pyridin-4-yl)-pyrrolidin-1-yl-methanoneHCID 59678084—

Reaction Steps

A mixture of the above aldehyde and sodium borohydride (400 mg, 10 mmol) in EtOH (50 mL) is stirred at room temperature for 1 hour. After evaporation of EtOH, EtOAc (40 mL) and water (40 mL) are added to the residue. The organic layer is separated, washed once with 1 N NaOH, 1N HCl and brine, dried (Na2SO4) and concentrated. The residue is chromatographed on silica gel (1:1 hexane:EtOAc) to give (2,6-dichloro-3-hydroxymethyl-pyridin-4-yl)-pyrrolidin-1-yl-methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07342115B2
Source datasetuspto-grants-2008_03
ORD IDord-ea2e78f9821e4ed48f0d73071e11677c
Source noteuspto-grants-2008_03