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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350183생성일: 2026년 10월 25일

Ethanol → 3-[1-(4-benzyloxybenzyl)-3-ethoxy-1H-pyrazol-4-yl]propionic acid

https://huagongshe.com/reaction/350183

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물TetrahydrofuranHCID 8028—
반응물Sodium HydroxideHCID 14798—
반응물ethyl 3-[1-(4-benzyloxybenzyl)-3-ethoxy-1H-pyrazol-4-yl]propionateHCID 23024769—
용매Hydrochloric AcidHCID 313—
생성물3-[1-(4-benzyloxybenzyl)-3-ethoxy-1H-pyrazol-4-yl]propionic acidHCID 6942073894.2%

반응 단계

A mixture of ethyl 3-[1-(4-benzyloxybenzyl)-3-ethoxy-1H-pyrazol-4-yl]propionate (490 mg), 1 N aqueous sodium hydroxide solution (3 ml), tetrahydrofuran (5 ml), and ethanol (5 ml) was stirred at room temperature for two hours, diluted with 1 N hydrochloric acid (3 ml), and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The obtained colorless crystals were collected by filtration, and 3-[1-(4-benzyloxybenzyl)-3-ethoxy-1H-pyrazol-4-yl]propionic acid (430 mg, yield: 94%) was obtained. This was recrystallized from acetone-hexane. Melting point: 115–116° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179823B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-1f07680b21844722a9d566a429fb24e7
출처 메모uspto-grants-2007_02