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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | 6-Hydroxy-1,3-dioxaindane-5-carbaldehyde | HCID 6710626 | — |
| Reactant | Nitroethanol | HCID 22056827 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6,7-Methylenedioxy-3-nitrochromene | HCID 57556941 | 61.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318938B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-de803bfe9ed44e0bb3284dd90dbc69b0 |
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| Source note | uspto-grants-2012_11 |
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