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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370435생성일: 2026년 10월 25일

Sulfuric Acid → [6-(Hydroxymethyl)pyridin-3-yl]methanol

https://huagongshe.com/reaction/370435

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Diethyl 2,5-pyridinedicarboxylateHCID 254728—
반응물Sodium borohydrideHCID 4311764—
반응물Calcium ChlorideHCID 5284359—
용매EthanolHCID 702—
생성물[6-(Hydroxymethyl)pyridin-3-yl]methanolHCID 82025151%

반응 단계

To a solution of 33.5 g (0.15 mol) of diethyl pyridine-2,5-dicarboxylate in 300 mL of absolute EtOH was added 11.4 g (0.3 mol) of NaBH4 in several portions over a 30-min period. Then a solution of 33.3 g (0.3 mol) of anhydrous CaCl2 in 200 ml of EtOH was added dropwise over a 1-h period. The mixture was stirred at room temperature for 16 h, and then it was neutralized with 12 to 13 mL of concentrated H2SO4. The CaSO4, which precipitated, was removed by centrifugation (two EtOH washings). The combined supernatant was concentrated, dissolved in about 10 mL of H2O, and applied to a 4.5×18-cm column of Dowex 50W-X8 cation exchange resin (H+ form). The column was eluted with H2O until the eluate was no longer acidic, and then it was eluted with dilute NH4OH, which removed the 2,5-pyridinedimethanol from the column. Evaporation afforded 10.6 g (51% yield) of 2,5-pyridinedimethanol as a light brown hygroscopic solid: 1H NMR (Me2SO-d6) δ4.55 and 4.59 (2 s, 4, CH2OH), 5.23 (broad s, 2, CH2OH), 7.42 (d, J=8 Hz, 1, 3'--H), 7.72 (dd, J=2 Hz, J=8 Hz, 1, 4--H), 8.42 (d, J=2 Hz, 1, 6'--H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04526787
출처 데이터셋uspto-grants-1985_07
ORD IDord-ed760393c94e4fd9b01c9a8a64d4c7c2
출처 메모uspto-grants-1985_07