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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471057Generated: November 2, 2026

Sodium borohydride → 1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diol

https://huagongshe.com/reaction/1471057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1,4-Bis(6-chloropyridin-3-yl)butane-1,4-dioneHCID 59617025—
SolventEthanolHCID 702—
Product1,4-Bis(6-chloropyridin-3-yl)butane-1,4-diolHCID 5961717189.2%

Reaction Steps

The product from Example 207A (2.90 g, 9.38 mmol) and sodium borohydride (0.745 g, 19.70 mmol) were combined in ethanol (94 mL) at 0° C. The mixture was warmed to room temperature and stirred for 6 hours. The solvent was evaporated and the residue was partitioned between ethyl acetate and 1M HCl. The organic layer was washed with water, brine, dried with sodium sulfate, filtered and evaporated to give the title compound (2.62 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006387B2
Source datasetuspto-grants-2015_04
ORD IDord-5ebc77ca5fe24590a74fd3459e59a848
Source noteuspto-grants-2015_04