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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501540Generated: October 25, 2026

8-Methylquinoline → 8-Methyl-5-nitroquinoline

https://huagongshe.com/reaction/501540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-MethylquinolineHCID 11910—
ReactantPotassium NitrateHCID 24434—
SolventSulfuric AcidHCID 1118—
Product8-Methyl-5-nitroquinolineHCID 24630094%

Reaction Steps

To a solution of commercially available 8-methylquinoline (5.0 g, 34 mmol) in concentrated H2SO4 (19 mL) at 0° C. was added portionwise KNO3 (4.29 g, 42.4 mmol). After the addition, the reaction was stirred at rt for 17 h, then poured into ice/water and extracted with EtOAc (3×100 mL). The aqueous layer was basified to pH=9 with solid Na2CO3 and extracted with EtOAc (2×100 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was chromatographed (silica gel) to yield the title compound (5.98 g, 94%) as a light yellow solid. LC/MS m/z 189 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772267B2
Source datasetuspto-grants-2010_08
ORD IDord-ec1720b845dd4c2ca42263c55fcb645d
Source noteuspto-grants-2010_08