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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2221871생성일: 2026년 10월 25일

Sodium sulfate decahydrate → {3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazol-4-yl}methanol

https://huagongshe.com/reaction/2221871

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참여 물질

역할이름HCID투입량
반응물Sodium sulfate decahydrateHCID 62649—
반응물Aluminium lithium hydrideHCID 21226445—
반응물ethyl 3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazole-4-carboxylateHCID 69217831—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물{3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazol-4-yl}methanolHCID 6921695761%

반응 단계

To a solution of ethyl 3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazole-4-carboxylate (7.54 g) in tetrahydrofuran (100 mL) was added lithium aluminum hydride (0.61 g) at 0° C. and the mixture was stirred at room temperature for 1 hr. Sodium sulfate decahydrate (5.19 g) was added to the reaction mixture and the mixture was stirred at room temperature for 30 min. The reaction mixture was diluted with ethyl acetate and the precipitate was filtered off, and the filtrate was concentrated. The residue was subjected to silica gel column chromatography to give {3-[(4-{[2-(2-furyl)-5-methyl-1,3-oxazol-4-yl]methoxy}-3-methoxybenzyl)oxy]-1-methyl-1H-pyrazol-4-yl}methanol as colorless crystals (4.15 g, yield 61%) from a fraction eluted with ethyl acetate-hexane (5:1, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 132-133° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07368578B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-5d8a199006b54c5ab9589526040da11e
출처 메모uspto-grants-2008_05