HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769546Generated: October 26, 2026
Hexane → Ethyl alpha-nitro-9H-thioxanthene-9-acetate
https://huagongshe.com/reaction/1769546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl nitroacetate | HCID 69379 | — |
| Reactant | 9H-thioxanthen-9-ol | HCID 5154170 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Ethyl alpha-nitro-9H-thioxanthene-9-acetate | HCID 15290759 | — |
Reaction Steps
Crude 9-hydroxythioxanthene (9.58 g, 45 mmol) is mixed with ethyl nitroacetate (5.5 mL, 49 mmol) and heated at 100° C. for 1 hour. TLC (SiO2, hexane:2-propanol/3:1) after 45 minutes shows no starting material. The cooled reaction mixture is treated with 100 mL of ethanol and 39 mL of 1.25M ethanolic potassium hydroxide solution. Ethanol is stripped and the residue taken up in water and extracted with diethyl ether. The aqueous layer is acidified to pH 2 to 3 with 85% phosphoric acid solution and refrigerated overnight. A crystalline solid is collected by filtration and dried at 50° C./10 mm Hg. A total of 8.4 g of the title compound is collected in three crops; mp 111°-115° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05380925 |
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| Source dataset | uspto-grants-1995_01 |
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| ORD ID | ord-f01a81cc0b12418786f7e3ff01829498 |
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| Source note | uspto-grants-1995_01 |
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