戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 927021作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/927021

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 6416458888.9%

反応手順

2.27 g of 4-benzyloxy-benzaldehydeoxime (10 mmol; 92% purity) was dissolved in 40 ml of methylenechloride (0.25 M), and 1.77 ml of propargyl alcohol (30 mmol) was then added to the resulting solution. 13.7 ml of 10% NaOCl (20 mmol) was then dropwise added very slowly to the resulting solution by using a dropping funnel at 0° C. After the addition of NaOCl was completed, the resulting mixture was stirred for about 5 hours while the temperature was slowly raised to room temperature. Subsequently, the completion of the reaction was confirmed by liquid chromatography, the resultant was subjected to distillation under reduced pressure to evaporate methylenechloride therefrom, 200 ml of water was added to the residue, and the obtained solid was then filtered. The filtered compound was washed with a large amount of water, and then washed with diethylether to obtain a solid compound. The obtained solid compound was purified with an ethylacetate/hexane solution (1:2) to obtain a white, solid [3-(4-benzyloxy-phenyl)-isoxazole-5-yl]-methanol (yield: 2.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09290464B2
出典データセットuspto-grants-2016_03
ORD IDord-2dff27191cb34109a4d5e951e8089697
出典メモuspto-grants-2016_03