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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612901Generated: October 29, 2026

3-(2-(N-tert-Butoxycarbonylamino)ethoxy)-4-(1-hydroxyisopropyl)-5-phenylisoxazole → 3-(2-Aminoethoxy)-4-isopropenyl-5-phenylisoxazole hydrochloride

https://huagongshe.com/reaction/612901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-(N-tert-Butoxycarbonylamino)ethoxy)-4-(1-hydroxyisopropyl)-5-phenylisoxazoleHCID 19596530—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Product3-(2-Aminoethoxy)-4-isopropenyl-5-phenylisoxazole hydrochlorideHCID 1959659383%

Reaction Conditions

Temperature100 °C

Reaction Steps

3-(2-(N-tert-Butoxycarbonylamino)ethoxy)-4-(1-hydroxyisopropyl)-5-phenylisoxazole (0.13 g) was dissolved in a 4N hydrochloric acid/1,4-dioxane solution (10 ml), and the solution was stirred at 100° C. for one hour. After the reaction, the reaction mixture was left to be cooled, followed by evaporation of the solvent under reduced pressure. The residue was washed with ethyl acetate to obtain the title compound (0.10 g, 83%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005116
Source datasetuspto-grants-1999_12
ORD IDord-f493ffc7cc574ba689329d75364963ae
Source noteuspto-grants-1999_12