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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1576894Generated: October 29, 2026

Ethanol → HCID 21509235, compound

https://huagongshe.com/reaction/1576894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
Reactant1H-Indene-1,3(2H)-dione, 2-nitro-HCID 77242—
ProductHCID 21509235HCID 21509235—

Reaction Steps

2-Nitroindane-1,3-dione (20.5g; 0.107 moles) in ethanol (100 ml) was heated under reflux for 4 hours, cooled, poured into water (1 liter). allowed to stand overnight and filtered. The solid was extracted with 5% sodium bicarbonate solution (3 × 100 ml) and filtered. The insoluble solid was predominantly the ψ-ethyl ester, 3-ethoxy-3-nitromethylphthalide, contaminated with some α-ethyl ester. Acidification of the combined sodium bicarbonate filtrates, filtration and recrystallisation from ethanol gave the α-ethyl ester, 2-ethoxycarbonyl-ω-nitroacetophenone, m.p. 81°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03983156
Source datasetuspto-grants-1976_09
ORD IDord-959f1727c99e470686ef06cc6689bea1
Source noteuspto-grants-1976_09