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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881719Generated: October 26, 2026

Phthalic Anhydride → 6,7-Methylenedioxy-3-nitrochromene

https://huagongshe.com/reaction/1881719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantDibutylamineHCID 8148—
Reactant6-Hydroxy-1,3-dioxaindane-5-carbaldehydeHCID 6710626—
ReactantNitroethanolHCID 22056827—
SolventDichloromethaneHCID 6344—
Product6,7-Methylenedioxy-3-nitrochromeneHCID 5755694161.2%

Reaction Steps

Aldehyde (2a) (6 g, 36.14 mmol) was dissolved in 300 ml of CH2Cl2 along with 3.1 ml of dibutylamine (18.16 mmol) and 10.72 g of phthalic anhydride in a two necked flask equipped with a Dean-Stark trap, a condenser and a dropping funnel. Nitroethanol (7 ml 97.69 mmol) was added dropwise over a period of 18 hours, while the solution was stirred at reflux. After addition, the reaction was stirred for an additional 24 hrs. The flask was then cooled to room temperature, filtered and the solution extracted with 2 M NaOH (300 ml×3) and brine (100 ml), then dried over MgSO4. The solvent was then evaporated to leave a concentrated solution which was passed through a short column of silica to remove dark polar impurities. The isolated material was recrystallized from methanol to give 4.89 g (61% yield) of the title compounds as red needles: mp 139° C.; 1H-NMR (CDCl3) δ 5.20 (s, 2, ArOCH2), 6.02 (s, 2, OCH2O), 6.49 (s, 1, ArH), 6.69 (s, 1, ArH), 7.75 (s, 1, ArCH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318938B2
Source datasetuspto-grants-2012_11
ORD IDord-de803bfe9ed44e0bb3284dd90dbc69b0
Source noteuspto-grants-2012_11