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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114543Generated: October 31, 2026

Nitric Acid → 5-bromo-3,4-dihydro-8-nitro-2H-naphthalen-1-one

https://huagongshe.com/reaction/2114543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSodium HydroxideHCID 14798—
Reactant5-Bromo-1,2,3,4-tetrahydronaphthalen-1-oneHCID 10889572—
SolventSulfuric AcidHCID 1118—
Product5-bromo-3,4-dihydro-8-nitro-2H-naphthalen-1-oneHCID 19990790336.6%

Reaction Steps

To prepare this compound, 90% fuming nitric acid (0.115 gram, 0.165 mmol) was added to a solution of 5-bromo-3,4-dihydro-2H-naphthalen-1-one (0.34 g, 1.50 mmol) in 3 mL concentrated sulfuric acid at 0° C. After 45 minutes, the mixture was poured into ice, and 6 N aqueous sodium hydroxide (9 mL) was added very slowly. That mixture was extracted twice with EtOAc (40 mL each), and the two extracts were combined. The combined EtOAc extract was washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting solid was subjected to flash chromatography (40% EtOAc/hexanes) and recrystallization (EtOAc/hexanes) to afford 0.15 g (38%) of 5-bromo-3,4-dihydro-8-nitro-2H-naphthalen-1-one. 1H NMR (500 MHz, CDCl3) δ 7.84 (d, J=8.2, 1H), 7.25 (d, J=8.2, 1H), 3.07 (t, J=6.2, 2H), 2.74 (t, J=6.7, 2H), 2.18-2.25 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435733B2
Source datasetuspto-grants-2008_10
ORD IDord-08e268109c4b48ce85098d2562fe0388
Source noteuspto-grants-2008_10