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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369758Generated: October 23, 2026

Nitric Acid → 2,3,8,9-Tetramethoxybenzo[i]phenanthridine

https://huagongshe.com/en/reaction/369758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantBenzene, 4-bromo-1,2-dimethoxy-HCID 76114—
Reactant4-Bromo-5-nitroveratroleHCID 170968—
SolventAcetic AcidHCID 176—
Product2,3,8,9-Tetramethoxybenzo[i]phenanthridineHCID 988472392%

Reaction Conditions

Temperature10 °C

Reaction Steps

3,4-Dimethoxy-6-nitro-bromobenzene (16). 3,4-Dimethoxybromobenzene (5 g, 23 mmol) was slowly added to a stirred solution of 35 mL concentrated nitric acid and 105 mL glacial acetic acid maintained at 10° C. The reaction mixture was stirred at 15° C. for 1 h and then diluted with 200 mL ice cold water. The resulting mixture was extracted thrice with 200 mL portions of ether. The combined organic phase was dried and evaporated in vacuo. The crude product was recrystallized from ethanol to give bright yellow needle shaped crystals of compound 16 in 92% yield; mp=122-124° C.; IR (Nujol) 1510, 1312; 1H NMR δ 3.94 (3H, s), 3.97 (3H, s), 7.12 (1H, s), 7.57 (1H, s); 13C NMR δ 56.9, 57.2, 108.0, 109.5, 117.0, 148.7, 153.3; Anal. calcd for C8H8NO4Br: C, 36.72, H, 3.14, N, 5.30; Found: C, 36.70, H, 3.13, N, 5.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140328
Source datasetuspto-grants-2000_10
ORD IDord-c1ca8439c99c47b08db926ebbb9216b9
Source noteuspto-grants-2000_10