HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(2-(N-tert-butoxycarbonylamino)ethoxy)-5-phenylisoxazole → 3-(2-Aminoethoxy)-5-phenylisoxazole hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(2-(N-tert-butoxycarbonylamino)ethoxy)-5-phenylisoxazole | HCID 15434960 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | 3-(2-Aminoethoxy)-5-phenylisoxazole hydrochloride | HCID 9859596 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06005116 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-c46849b2fb8e45e693db535177303647 |
| Source note | uspto-grants-1999_12 |