HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258193Generated: October 30, 2026
Isopropanol → alpha-Amino-9H-thioxanthene-9-acetic acid, hydrochloride
https://huagongshe.com/reaction/258193
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl alpha-amino-9H-thioxanthene-9-acetate hydrochloride | HCID 67804420 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | alpha-Amino-9H-thioxanthene-9-acetic acid, hydrochloride | HCID 67803772 | 18.5% |
Reaction Steps
Ethyl α-amino-9H-thioxanthene-9-acetate hydrochloride (3.5 g, 10 mmol) is dissolved in 30 mL of absolute ethanol and 33 mL of 1.25 M ethanolic potassium hydroxide solution (4 equivalents) is added. The reaction mixture is stirred at room temperature for 22 hours when TLC (SiO2, hexane:2-propanol/3:1) shows no starting material. Ethanol is stripped under vacuum and the residue taken up in 75 mL of water and extracted with diethyl ether. The aqueous solution is acidified with 1N hydrochloric acid to pH 7 and a precipitate is collected by filtration, washed with water, dried at 45° C./2 mm Hg over phosphorous pentoxide (P2O5). This gives 1.65 g of the title compound; mp 244°-246° C. The mother liquor is concentrated, cooled at +3° C. to furnish the second crop (0.57 g) of the title compound as a hydrochloride free base mixture. The above solids are combined in 50 mL of water and treated with 1N hydrochloric acid to pH 1. The mixture is stripped to dryness under vacuum and the residue dried at 50° C./2 mm Hg to give the title compound; mp 269°-273° C. (dec).
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-c05e363cd3b74c1ebf123f047a03c022 |
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| Source note | uspto-grants-1993_11 |
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