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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 927021생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl alcoholHCID 7859—
반응물4-Benzyloxy-benzaldehyde oximeHCID 763359—
반응물Sodium HypochloriteHCID 23665760—
용매DichloromethaneHCID 6344—
생성물[3-(4-Benzyloxy-phenyl)-isoxazol-5-yl]-methanolHCID 6416458888.9%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290464B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-2dff27191cb34109a4d5e951e8089697
출처 메모uspto-grants-2016_03