HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258191Generated: October 26, 2026
Hexane → Ethyl alpha-nitro-9H-thioxanthene-9-acetate
https://huagongshe.com/reaction/258191
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 1.25 M 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 | US05264577 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-5692cc207ef046b3ad5043b7e9a3a092 |
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| Source note | uspto-grants-1993_11 |
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