Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065641Generated: October 29, 2026

Sodium borohydride → HCID 20539683, compound

https://huagongshe.com/reaction/1065641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 12923248HCID 12923248—
SolventMethanolHCID 887—
ProductHCID 20539683HCID 20539683706.2%

Reaction Steps

8.7 g (0.025 mol) of 1-(6-chloro-pyridin-2-yl-oxy)-2-(4-chlorophenyl)-1-(1,2,4-triazol-1-yl)-ethan-2-one (Example 1) were dissolved in 100 ml of methanol, and 1 g (0.025 mol) of sodium borohydride was added. The mixture was heated under reflux for 30 minutes and concentrated by distilling off the solvent in vacuo, and the residue was partitioned between chloroform and water. The organic phase was separated off, extracted again by shaking with water, dried over magnesium sulphate and concentrated. 62 g (70% of theory) of 1-(6-chloro-pyridin-2-yl-oxy)-2-(4-chlorophenyl)-1-(1,2,4-triazol-1-yl)-ethan-2-ol were obtained as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04330547
Source datasetuspto-grants-1982_05
ORD IDord-19d5e13f00294dfb894f361c318806ee
Source noteuspto-grants-1982_05