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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7145생성일: 2026년 10월 24일

Diisobutylaluminum hydride → 3-Propoxypicolinaldehyde

https://huagongshe.com/ko/reaction/7145

반응식

참여 물질

역할이름HCID투입량
반응물Diisobutylaluminum hydrideHCID 14487—
반응물Potassium sodium tartarateHCID 9855836—
반응물Propyl 3-Propoxypyridine-2-carboxylateHCID 19756120—
촉매Manganese dioxideHCID 14801—
용매DichloromethaneHCID 6344—
생성물3-PropoxypicolinaldehydeHCID 22018851113.5%

반응 조건

온도-78 °C

반응 단계

To a stirred solution of 3-n-propoxypicolinic acid n-propyl ester (0.1209 g, 0.541 mmol) in dry CH2Cl2 (5 mL) at −78° C. was added DIBAL-H (1.0 M, 2.5 mL, 2.5 mmol). The mixture was stirred at −78° C. for 1 hr, then at room temperature for 3 hrs. The mixture was poured into saturated aqueous sodium potassium tartrate (15 mL), diluted with CH2Cl2 (15 mL) and stirred vigorously for 65 hrs. The phases were separated and the aqueous phase extracted with CH2Cl2 (3×20 mL). The combined organic phases were dried (Na2SO4) and concentrated to give a yellow oil. The yellow oil was dissolved in CH2Cl2 (5 mL) and treated with MnO2 (˜85%, 0.4549 g, 4.45 mmol). The mixture was stirred for 19 hrs then filtered through celite. The filtrate was concentrated to give 0.1014 g of 3-n-propoxypyridine-2-carboxaldehyde as an orange oil. 1H NMR (CDCl3) d 1.09 (t, 3H, J=7.4 Hz), 1.91 (sextet, 2H, J=7.1 Hz), 4.07 (t, 2H, J=6.6 Hz), 7.38–7.47 (m, 2H), 8.39 (dd, 2H, J=4.4, 1.4 Hz), 10.43 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084155B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-41a445326c2b4979809438ee5d7e9725
출처 메모uspto-grants-2006_08