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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356958생성일: 2026년 10월 26일

Diisopropylamine → 4-[2-(3-Cyclopentyloxy-4-methoxyphenyl)-2-hydroxyethyl]pyridine

https://huagongshe.com/reaction/356958

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물4-MethylpyridineHCID 7963—
반응물Ammonium ChlorideHCID 25517—
반응물3-Cyclopentyloxy-4-methoxybenzaldehydeHCID 2735893—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-[2-(3-Cyclopentyloxy-4-methoxyphenyl)-2-hydroxyethyl]pyridineHCID 2214585791.1%

반응 조건

온도70 °C

반응 단계

A stirred solution of diisopropylamine (14 mL) in dry tetrahydrofuran (150 mL), is treated dropwise with a solution of butyl lithium in hexanes (40 mL; 2.5 M), under nitrogen, while keeping the temperature at below -70° C. The resulting mixture is then stirred for a further period of 30 minutes at below - 70° C. The stirred mixture, while it is still maintained at below -70° C., is then treated dropwise with a solution of 4-picoline (9.3 g) in dry tetrahydrofuran (20 mL). The stirred mixture is maintained at below -70° C. for a further 45 minutes. The stirred mixture, while it is still maintained at below -70° C., is then treated with a solution of 3-cyclopentyloxy-4-methoxybenzaldehyde (22.0 g) in dry tetrahydrofuran (100 mL), and it is stirred at below -70° C. for a further 30 minutes. The resulting mixture is then allowed to warm to room temperature overnight, and then treated with saturated aqueous ammonium chloride solution (200 mL). The layers are separated and the aqueous layer is further extracted with ethyl acetate (3×300 mL). The combined organic extracts are dried over magnesium sulfate and evaporated to dryness. The resulting residue is recrystallized from ethyl acetate, to give (±)-1-(3-cyclopentyloxy-4-methoxyphenyl)-2-(pyrid-4-yl)ethanol (28.5 g), in the form of a cream solid, m.p. 102°-103° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840724
출처 데이터셋uspto-grants-1998_11
ORD IDord-409ea20b0c164f54bb826fa8585da341
출처 메모uspto-grants-1998_11