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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612857Generated: October 31, 2026

3-(2-(N-tert-butoxycarbonylamino)ethoxy)-5-phenylisoxazole → 3-(2-Aminoethoxy)-5-phenylisoxazole hydrochloride

https://huagongshe.com/reaction/612857

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-(N-tert-butoxycarbonylamino)ethoxy)-5-phenylisoxazoleHCID 15434960—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Product3-(2-Aminoethoxy)-5-phenylisoxazole hydrochlorideHCID 985959699%

Reaction Steps

A solution of 4N hydrochloric acid/1,4-dioxane (4.0 ml) was added to 3-(2-(N-tert-butoxycarbonylamino)ethoxy)-5-phenylisoxazole (0.50 g), and the mixture was stirred at room temperature for 15 minutes. The precipitate was separated from the mixture by filtration and washed with ethyl acetate to obtain the title compound (0.39 g, 99%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06005116
Source datasetuspto-grants-1999_12
ORD IDord-c46849b2fb8e45e693db535177303647
Source noteuspto-grants-1999_12