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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 871477생성일: 2026년 10월 26일

Hydrochloric Acid → 5-(Propan-2-yl)-1,2-oxazol-3-amine

https://huagongshe.com/reaction/871477

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N'-hydroxy-2-(2-isopropyl-1,3-dioxolan-2-yl)acetimidamideHCID 86653514—
용매EthanolHCID 702—
생성물5-(Propan-2-yl)-1,2-oxazol-3-amineHCID 1333466368%

반응 조건

온도120 °C

반응 단계

N′-Hydroxy-2-(2-isopropyl-1,3-dioxolan-2-yl)acetimidamide (1.8 g, 9.57 mmol) was dissolved in ethanol (12 ml) and acidified to pH=1 with 37% aqueous hydrochloric acid. The mixture was subjected to microwave heating at 120° C. for 30 minutes. After concentration under reduced pressure the residue was diluted with dichloromethane, a solution of saturated sodium bicarbonate was added until the solution became basic (pH=11) and the organic layer separated. After multiple extractions of the water phase with dichloromethane, the organic layers were combined, dried (MgSO4), filtered and concentrated under reduced pressure. The crude material was purified by silica gel chromatography (hexane/ethyl acetate 1:1) to afford 5-isopropylisoxazol-3-amine (819 mg, 68%). 1H NMR (300 MHz, CDCl3) δ 5.52 (s, 1H), 3.89 (bs, 2H), 2.96-2.91 (m, 1H), 1.27 (d, 6H); LC-MS (ESI) m/z 127 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08969587B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-dd18d9e6235c4207b586b74d22d8a020
출처 메모uspto-grants-2015_03