Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073943Generated: October 26, 2026

Sodium hydride → 5-benzyloxy-2-[3-(4-cyanophenoxy)-3-methyl-1-butenyl]pyridine N-oxide

https://huagongshe.com/reaction/1073943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 54352845HCID 54352845—
SolventIsopropanolHCID 3776—
Product5-benzyloxy-2-[3-(4-cyanophenoxy)-3-methyl-1-butenyl]pyridine N-oxideHCID 54393685121.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

1.69 g of 5-benzyloxy-2-[3-(4-cyanophenoxy)-3-methyl-2-(methylsulphonyloxy)butyl]pyridine N-oxide were added to a solution of 0.14 g of 80% sodium hydride in 15 ml of isopropanol and the solution was stirred at 20° C. for 16 hours. The solvent was then removed by evaporation and the residue was partitioned between ethyl acetate and sodium chloride solution The organic phase was washed with sodium chloride solution and then evaporated to give 1.64 g of 5-benzyloxy-2-[3-(4-cyanophenoxy)-3-methyl-1-butenyl]pyridine N-oxide in the form of a pale cream solid of melting point 125° C. after recrystallization from ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971982
Source datasetuspto-grants-1990_11
ORD IDord-01901d3d01a74a379136972f67d9cd0b
Source noteuspto-grants-1990_11