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HRID 72313作成日:2026年10月24日

Propargyl alcohol → [3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanol

https://huagongshe.com/ja/reaction/72313

反応式

関与物質

役割名称HCID仕込み量
反応物Propargyl alcoholHCID 7859—
反応物4-Benzyloxy-benzaldehyde oximeHCID 763359—
反応物Sodium HypochloriteHCID 23665760—
溶媒DichloromethaneHCID 6344—
生成物[3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanolHCID 64164588—

反応手順

4-benzyloxy-benzaldehyde oxime (2.27 g, 10 mmol-a compound of 92% purity) was dissolved in methylene chloride (40 ml, 0.25 M), to which solution was added propargyl alcohol (1.77 ml, 30 mmol). To the resulting solution was very slowly dropwise added 10% NaOCl (13.7 ml, 20 mmol) at 0° C., using a dropping funnel. After the addition of NaOCl was completed, the mixture was stirred for about 5 hours while increasing the temperature slowly to room temperature. The completion of the reaction was confirmed by liquid chromatography, and the mixture was distilled under reduced pressure to remove the methylene chloride. Water (200 ml) was added to the residue and the resulting solid was filtered off. The filtered compound was washed with excess of water and finally washed with diethyl ether. The thus-obtained solid compound was recrystallized from ethyl acetate/hexane (1:2) to obtain 2.50 g of [3-(4-benzyloxy-phenyl)-isoxazol-5-yl]-methanol as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828992B2
出典データセットuspto-grants-2014_09
ORD IDord-5fbbabaf954345bd939643f966166217
出典メモuspto-grants-2014_09