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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240359Generated: October 29, 2026

Water → N-(2-nitrophenyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-amine

https://huagongshe.com/reaction/240359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
Reactant1,4-Benzodioxan-6-ylamineHCID 89148—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(2-nitrophenyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-amineHCID 918596667.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

5.9 g (39 mmol) of 2,3-dihydrobenzo[b]1,4-dioxin-6-amine and 5.0 g (35 mmol) of 2-fluoronitrobenzene were dissolved in N-methylpyrrolidone (70 mL) and 20.8 g (150 mmol) of potassium carbonate was added thereto. The solvent was heated with stirring for 10 hours at 120° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The extracted organic layer was washed with water, 10% hydrochloric acid, water, and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue thus obtained was purified by silica gel chromatography (developing solvent: ethyl acetate:hexane=1:4), to obtain 6.4 g (yield: 66%) of N-(2-nitrophenyl)-2,3-dihydrobenzo[b][1,4]dioxin-6-amine as a red liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648075B2
Source datasetuspto-grants-2014_02
ORD IDord-404e472ffc854222b67e36eaaaf7dde9
Source noteuspto-grants-2014_02