HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21509235, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1H-Indene-1,3(2H)-dione, 2-nitro- | HCID 77242 | — |
| Product | HCID 21509235 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983156 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-959f1727c99e470686ef06cc6689bea1 |
| Source note | uspto-grants-1976_09 |