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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781859Generated: October 29, 2026

alpha-(3,4-Dimethoxy-5-nitrophenyl)-2-pyridinemethanol → 3,4-Dimethoxy-5-nitrophenyl 2-pyridyl ketone

https://huagongshe.com/reaction/1781859

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-(3,4-Dimethoxy-5-nitrophenyl)-2-pyridinemethanolHCID 21459111—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
Product3,4-Dimethoxy-5-nitrophenyl 2-pyridyl ketoneHCID 17977723—

Reaction Steps

7 g of manganese dioxide and added portionwise to 4.0 g of α-(3,4-dimethoxy-5-nitrophenyl)-2-pyridine-methanol dissolved in 100 ml of acetone while constantly heating under reflux over a period of 2.5 hours. Thereupon, the mixture is heated under reflux for an additional 2 hours. The manganese salts are subsequently filtered and the residue obtained after evaporation is recrystallized from ether/hexane. There is obtained 3,4-dimethoxy-5-nitrophenyl 2-pyridyl ketone of m.p. 113°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633371
Source datasetuspto-grants-1997_05
ORD IDord-138571790bae4b9aa8198da6b9657a45
Source noteuspto-grants-1997_05