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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 606201생성일: 2026년 10월 24일

Water → (1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanol

https://huagongshe.com/ko/reaction/606201

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ethyl AcetateHCID 8857—
반응물1,3-DihydroisobenzofuranHCID 10327—
반응물1-Benzylpiperidine-4-carbaldehydeHCID 89584—
용매TetrahydrofuranHCID 8028—
용매ButyllithiumHCID 178418339—
생성물(1-Benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanolHCID 2224846537.5%

반응 조건

온도-70 °C

반응 단계

After dissolving 591 mg of 1,3-dihydroisobenzofuran in 10 ml of tetrahydrofuran, 3.9 ml of n-butyllithium (1.5 M, n-hexane solution) was added thereto at −70° C. under a nitrogen atmosphere, the mixture was stirred for 1 hour, and then a solution of 1 g of 1-benzylpiperidine-4-carboxaldehyde in tetrahydrofuran (5 ml) was added dropwise and the mixture was stirred for 1 hour. Water was added to the reaction solution, extraction was performed with ethyl acetate, the extract was dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. Purification was performed by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain 597 mg of (1-benzylpiperidin-4-yl)-(1,3-dihydroisobenzofuran-1-yl)methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07915274B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-3cdf1cd5e0934747a1a5feee8f3dbe3e
출처 메모uspto-grants-2011_03