HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258189Generated: October 30, 2026
Hexane → alpha-Amino-9H-xanthene-9-acetic acid hydrochloride
https://huagongshe.com/reaction/258189
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl alpha-amino-9H-xanthene-9-acetate hydrochloride | HCID 67803757 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | alpha-Amino-9H-xanthene-9-acetic acid hydrochloride | HCID 67805111 | — |
Reaction Steps
Ethyl α-amino-9H-xanthene-9-acetate hydrochloride (5.33 g, 17 mmol) is combined with 45 mL of absolute ethanol and 27 mL of 1.25 M ethanolic potassium hydroxide solution (2 equivalents). The progress of the reaction is monitored by thin layer chromatography (TLC), silica gel (SiO2), hexane:2-propanol/3:7 with 1% of acetic acid. After 13 hours and an additional two equivalents of the potassium hydroxide solution (in three portions) most of the starting material is consumed. Ethanol is stripped off, the residue is taken up in 100 mL of water, and extracted with diethyl ether. The aqueous portion is acidified with 0.5 N hydrochloric acid (~100 mL) to pH 2 and cooled overnight. A white precipitate is collected by filtration, washed with cold water, diethyl ether, and dried at 50° C./10 mm Hg. This provides 3.18 g of the title compound; mp 264°-269° 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-76d56e6e42974ab5b2a0fd50c3140a0b |
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| Source note | uspto-grants-1993_11 |
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