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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7406생성일: 2026년 10월 24일

Hexane → 1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OL

https://huagongshe.com/ko/reaction/7406

반응식

참여 물질

역할이름HCID투입량
반응물HexaneHCID 8058—
반응물1-Benzyl-4-piperidoneHCID 19220—
반응물1-(1-Phenylethyl)-1h-imidazoleHCID 9815351—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물1-Benzyl-4-(1-phenethyl-1H-imidazol-2-YL)piperidin-4-OLHCID 1132590475%

반응 조건

온도-70 °C

반응 단계

A mixture of DIPA (1.4 mol) in THF (3000 ml) was stirred at −70° C. under N2 flow. Butyllithium 2.5 M/hexane (1.3 mol) was added portionwise at a temperature below −40° C. The mixture was stirred at −70° C. for 15 min. 1-phenylethyl-1H-imidazole (1 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour. 1-(phenylmethyl)-4-piperidinone (1.2 mol) dissolved in THF was added dropwise at a temperature below −55° C. The mixture was stirred at −70° C. for 1 hour, then brought to room temperature, stirred at room temperature overnight and decomposed with H2O. The organic solvent was evaporated. The aqueous concentrate was extracted with CH2Cl2. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from DIPE (1100 ml). The precipitate was filtered off, washed with DIPE and dried, yielding 271 g of 4-[1-(2-phenylethyl)-1H-imidazol-2-yl]-1-(phenylmethyl)-4-piperidinol (75%) (interm. 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087595B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-b62c82ce4a9f497c902d1d7f12e1a2c2
출처 메모uspto-grants-2006_08