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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1061880생성일: 2026년 10월 27일

Toluene → 6-[1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]-N,N-diisopropyl-2-naphthamide

https://huagongshe.com/reaction/1061880

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물isopropyl(1-trityl-1H-imidazol-4-yl)ketoneHCID 10150490—
반응물6-bromo-N,N-diisopropyl-2-naphthamideHCID 21879639—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물6-[1-hydroxy-2-methyl-1-(1-trityl-1H-imidazol-4-yl)propyl]-N,N-diisopropyl-2-naphthamideHCID 2228506389.6%

반응 단계

To a solution of toluene (1000 mL) containing a solution (1.6 M : 98.3 mL) of butyllithium in hexane was dropwise added a solution (250 mL) of 6-bromo-N,N-diisopropyl-2-naphthamide (50.0 g) in THF at −70° C. The mixture was stirred at the same temperature for 30 min., and a solution (200 mL) of 2-methyl-1-(1-trityl-1H-imidazol-4-yl)-1-propanone (47.5 g) in THF was added dropwise. The mixture was stirred for 20 min. Water was added and the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated and the residue was recrystallized from isopropyl ether to give the title compound (71.1 g) as a colorless powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06960586B2
출처 데이터셋uspto-grants-2005_11
ORD IDord-c6d69dfcdc694d08b1f0d374062b7e15
출처 메모uspto-grants-2005_11