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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199407Generated: October 30, 2026

Nitric Acid → HCID 59003390, compound

https://huagongshe.com/reaction/2199407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13495811HCID 13495811—
SolventSulfuric AcidHCID 1118—
ProductHCID 59003390HCID 59003390—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2,2,6-trimethyl-1,2,3,4-tetrahydroquinoline (0.66 g, 3.8 mmol) in 10 mL of concentrated sulfuric acid was cooled to 0° C. in an ice bath. To this solution was added dropwise 1.0 mL 90% fuming nitric acid. The resulting mixture was stirred at 0° C. for 30 min, poured onto 150 mL of ice-water, neutralized to pH=7 with K2CO3 and extracted with CH2Cl2 (3×200 mL). The combined organic layers were washed with water (2×300 mL), saturated aqueous NaHCO3 (300 mL) and brine (300 mL) The solution was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography (Silica gel, 15 to 20% ethyl acetate/hexane gradient elution) to give 2,2,6-trimethyl-7-nitro-1,2,3,4-tetrahydroquinoline. 1H NMR (500 MHz, CDCl3): 8.03 (s, 1H), 7.05 (s, 1H), 2.85 (td, J=6.6, 1.1 Hz, 2H), 2.17 (s, 3H), 1.76 (t, J=6.6 Hz, 2H), 1.35 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359285B2
Source datasetuspto-grants-2016_06
ORD IDord-8e3cd461e60d4ef3a8e9e9860f43cbe8
Source noteuspto-grants-2016_06