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HRID 631432作成日:2026年10月25日

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

https://huagongshe.com/reaction/631432

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物N'-hydroxy-2-(2-isopropyl-1,3-dioxolan-2-yl)acetimidamideHCID 86653514—
溶媒EthanolHCID 702—
生成物5-(Propan-2-yl)-1,2-oxazol-3-amineHCID 1333466368%

反応条件

温度120 °C

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09320739B2
出典データセットuspto-grants-2016_04
ORD IDord-ca7a53d0849545f28aa7318a67e8f941
出典メモuspto-grants-2016_04