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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600438Generated: October 29, 2026

Sodium borohydride → HCID 5148089, compound

https://huagongshe.com/reaction/1600438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-CYANO-1-METHYLPYRIDINIUM IODIDEHCID 11207327—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 5148089HCID 5148089—

Reaction Steps

To a solution of 2 (133 g, 0.54 mol) in methanol (1000 ml) and water (200 ml) was added sodium borohydride (41 g, 1.08 mol) in portions at temperatures below 28° C. After the addition the mixture was stirred for 1 hour at room temperature. Most of the methanol was distilled off. To the residue was added saturated ammonium chloride solution (200 ml), and the mixture was extracted three times with ether (300 ml). The combined organ phases wee washed once with water and were then extracted three times with 4M hydrochloric and (300 ml). The colored aqueous phases were kept for 1 hour at room temperature, and pH was then adjusted to 14. The mixture was extracted three times with ether (250 ml), and the combined organic phases were separated from the solid byproducts. The organic phase was washed with 4 portions of saturated sodium chloride solution (200 ml), dried over magnesium sulphate and evaporated. This yielded 17.4 g (0.143 mol, 26%) of crude oily title compound, which was sufficiently pure according to the 1H NMR spectrum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE036374
Source datasetuspto-grants-1999_11
ORD IDord-f8503d880bc54c7aa1338d7af4bb25ff
Source noteuspto-grants-1999_11