Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086579Generated: October 30, 2026

1,4-Dioxane → HCID 135515429, compound

https://huagongshe.com/reaction/2086579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 10354455HCID 10354455—
CatalystNickelHCID 935—
ProductHCID 135515429HCID 13551542924.4%

Reaction Steps

2-Amino-6-benzylamino-3-nitropyridine (25 g, 0.10 mol) was hydrogenated under 5.5 bar of H2 in the presence of 10 g of Raney-Ni in 400 mL of dioxane at 60 C. After 2 hours the reaction mixture was cooled to room temperature, filtrated and 4-hydroxy phenylglyoxal was added and stirred for 2 hours under an argon atmosphere. The suspension was then diluted with water, the solid was collected by filtration, washed with water, recrystallized from 2-propanol, and dried at 50 C in vacuo to give 6-benzylamino-3-(4-hydroxyphenyl)-5-azaquinoxaline (8 g, 24.4%, m.p. 271-273 C).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727252B1
Source datasetuspto-grants-2004_04
ORD IDord-f2a9216349a24d0db5a7e39eb1dce111
Source noteuspto-grants-2004_04