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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 712687생성일: 2026년 10월 27일

Methyl iodide → 3-Bromo-5-(2-methoxypropan-2-yl)pyridine

https://huagongshe.com/reaction/712687

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium hydrideHCID 24758—
반응물2-(5-Bromo-3-pyridyl)propan-2-olHCID 22391966—
용매DimethylformamideHCID 6228—
생성물3-Bromo-5-(2-methoxypropan-2-yl)pyridineHCID 6678813469.8%

반응 조건

온도0 °C

반응 단계

To a mixture of NaH (240 mg, 6.02 mmol) in DMF (dry, 4 mL) at 0° C. is added the solution of 2-(5-bromo-pyridin-3-yl)-propan-2-ol (500 mg, 2.31 mmol) in DMF (dry, 4 mL). The mixture is stirred at 0° C. for 15 min then raised to room temperature and stirred for 1 h. The mixture is then cooled back to 0° C. and iodomethane (397 mg, 2.80 mmol) iss added. The reaction mixture is stirred at room temperature overnight and is quenched by adding water dropwise. The mixture is partitioned between DCM and water. The DCM phase is separated and then washed with water twice. The DCM phase is evaporated under high vacuum. The residue is separated by silica gel flash column (EtOAc/Hepane 0 to 40% gradient, then 40%) to obtain 371 mg 3-bromo-5-(1-methoxy-1-methyl-ethyl)pyridine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181272B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-3af60b42a4b848ca8fb5e516774f8b2f
출처 메모uspto-grants-2015_11