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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1765076생성일: 2026년 10월 26일

tert-Butanol → 2-({2-[2-(Dimethylamino)-2-methylpropoxy]pyridin-3-yl}oxy)ethanol

https://huagongshe.com/reaction/1765076

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참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물2-(Dimethylamino)-2-methylpropanolHCID 23435—
반응물2-Chloro-3-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]pyridineHCID 21106670—
반응물Potassium tert-butoxideHCID 23665647—
용매TolueneHCID 1140—
생성물2-({2-[2-(Dimethylamino)-2-methylpropoxy]pyridin-3-yl}oxy)ethanolHCID 2110665380%

반응 조건

온도50 °C

반응 단계

A solution of 2-chloro-3-[2-(tetrahydro-2H-pyran-2-yloxy)ethoxy]pyridine (from Example 4; 100 mg, 0.39 mmol), 2-(dimethylamino)-2-methyl-1-propanol (68 μl, 0.58 mmol) and 1.0 M potassium tert-butoxide in tert-butanol (0.8 mL, 0.80 mmol) in 4 mL of toluene was heated at 100° C. for 1 day. The organic phase was washed with 3×2 mL of water and 2 mL of brine. The organic phase was shaken at 50° C. with 4 mL of 2.0 M acetic acid for 2 days. The aqueous phase was washed with 3×3 mL of ethyl acetate, made basic by addition of potassium hydroxide, saturated with sodium chloride and extracted with 3×2 mL of ethyl acetate. The organic phase was dried (MgSO4) and concentrated under reduced pressure to give 79 mg (0.31 mmol, 80%) of the title compound as a colorless oil. LC-UV purity 95%. MS m/z 255 (M+1)+, calc. 255 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07226925B2
출처 데이터셋uspto-grants-2007_06
ORD IDord-626d26ecca7c42f6baf70793cb92c265
출처 메모uspto-grants-2007_06