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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769544Generated: November 2, 2026

Hexane → alpha-Amino-9H-xanthene-9-acetic acid hydrochloride

https://huagongshe.com/reaction/1769544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl alpha-amino-9H-xanthene-9-acetate hydrochlorideHCID 67803757—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Productalpha-Amino-9H-xanthene-9-acetic acid hydrochlorideHCID 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 1.25M 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 0.5N 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05380925
Source datasetuspto-grants-1995_01
ORD IDord-18e710001f9e4e49af987f55b55e07ba
Source noteuspto-grants-1995_01