돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1618생성일: 2026년 10월 24일

Propargyl bromide → Methyl-3-propargyloxy-2-naphthoate

https://huagongshe.com/ko/reaction/1618

반응식

참여 물질

역할이름HCID투입량
반응물Propargyl bromideHCID 7842—
반응물Sodium hydrideHCID 24758—
반응물Methyl 3-hydroxy-2-naphthoateHCID 70163—
용매TetrahydrofuranHCID 8028—
생성물Methyl-3-propargyloxy-2-naphthoateHCID 5426244635%

반응 단계

Methyl-3-hydroxy-2-naphthoate (2.63 g, 0.013 mol) was dissolved in dry THF (80 ml) and treated with sodium hydride (80%) ((0.398 g, 0.013 mol), with stirring under N2. After 0.5 h, propargyl bromide (80% in toluene) (2.57 ml 0.017 mol) was added and the mixture heated to reflux. After 20 h, the reaction mixture was allowed to cool and then evaporated under reduced pressure. The residue was then evaporated under reduced pressure. The residue was then partitioned between EtOAc and water. The aqueous layer was then extracted with EtOAc (1×), and the combined organic layers were dried (Na2SO4) and evaporated to given an orange oil. Crystallisation of the oil from petrol (60/80) diethyl ether provided the title compound as a pale yellow solid (1.0 gg, 35%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726187
출처 데이터셋uspto-grants-1998_03
ORD IDord-33fdd502bd9b4b6ab4abded4f14a5ab2
출처 메모uspto-grants-1998_03