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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073910Generated: November 3, 2026

Sodium borohydride → HCID 54509110, compound

https://huagongshe.com/reaction/1073910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53697095HCID 53697095—
SolventEthanolHCID 702—
ProductHCID 54509110HCID 5450911096.6%

Reaction Steps

7.3 g of 2-[3-(4-cyanophenoxy)-3-methyl-2-oxobutyl]-6-methylpyridine N-oxide in 160 ml of ethanol were treated with 0.96 g of sodium borohydride and the mixture was stirred for 30 minutes. The solvent was removed by evaporation and the residue was taken up in water and dichloromethane. The organic phase was separated, dried over sodium sulphate and evaporated. The residue was crystallized from diethyl ether to give 7.1 g of 2-[3-(4-cyanophenoxy)-2-hydroxy-3-methylbutyl]-6-methylpyridine N-oxide of melting point 89°-92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971982
Source datasetuspto-grants-1990_11
ORD IDord-6db18914f448424d8fd33bb5b05d5ed6
Source noteuspto-grants-1990_11