HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769542Generated: October 26, 2026
Ethanol → Ethyl alpha-nitro-9H-xanthene-9-acetate
https://huagongshe.com/reaction/1769542
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl nitroacetate | HCID 69379 | — |
| Reactant | Xanthydrol | HCID 72861 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl alpha-nitro-9H-xanthene-9-acetate | HCID 15290758 | — |
Reaction Steps
9-Hydroxyxanthene (9.9 g, 50 mmol) and ethyl nitroacetate (6.1 mL, 55 mol) are mixed and heated at 100° C. (oil bath) for 1.5 hours. After cooling, a waxy mixture is suspended in 40 mL of absolute alcohol and 40 mL of 1.25M of ethanolic potassium hydroxide solution is added. The solution is stirred for 45 minutes at room temperature and ethanol is stripped off. The remaining solid is suspended in water and extracted with diethyl ether. The aqueous portion is acidified with 85% phosphoric acid to pH 2 to 3 to give a white suspension which is cooled overnight. The precipitate is collected by filtration and dried in a vacuum oven at 50° C. This gives 9.18 g of the title compound as a white solid; mp 89°-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05380925 |
|---|
| Source dataset | uspto-grants-1995_01 |
|---|
| ORD ID | ord-327004b003b141acbb54bf419399cd8d |
|---|
| Source note | uspto-grants-1995_01 |
|---|