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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595140Generated: October 29, 2026

Nitric Acid → HCID 86684831, compound

https://huagongshe.com/reaction/595140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 697934HCID 697934—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86684831HCID 8668483136.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(6,7,9,10,12,13-Hexahydro-5,8,11,14-tetraoxa-benzocyclododecen-2-yl)-ethanone (200 mmol, 51.3 g) dissolved in DCM (750 ml) and the mixture cooled to 0° C. Nitric acid (90%, 300 mmol, 14 ml) was added dropwise to the cooled solution over 20 minutes. Sulfuric acid (96.2%, 300 mmol, 8.75 ml) was then added dropwise over 40 minutes at 0° C. Additional nitric acid (200 mmol, 9.4 ml) was added dropwise over 20 minutes. The reaction mixture was diluted with water (300 ml) and wash with water (3×200 ml), Sat. NaHCO3 (4×200 ml, or until neutral). The organic layer was dried over Na2SO4 and concentrated. The crude mixture was recrystallized with DMF to give 22.5 g of the nitro product. The DMF layer was concentrated and recrystallized with ethyl acetate to give additional 8.75 g of the product. The ethyl acetate layer was concentrated and purified on silica column using 20% EtOAc/hexanes to give another 4.75 g of the product. Total yield is 36 g, (−60%). 1HNMR (400 MHz, DMSO) δ 7.82 (s, 1H), 7.61 (s, 1H), 4.35 (s, 4H), 3.87 (d, 4H), 3.62 (s, 4H), 2.71 (s, 3H). LC/MS Calcd for (M+H)−312.3. found 312.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242991B2
Source datasetuspto-grants-2016_01
ORD IDord-fbcc00a4044f49d3b2012fa7d662b59a
Source noteuspto-grants-2016_01