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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60806생성일: 2026년 10월 25일

Triethylamine → 2-(6-Methylpyridin-2-yl)ethyl methanesulfonate

https://huagongshe.com/reaction/60806

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물6-Methylpyridine-2-ethanolHCID 70283—
용매TolueneHCID 1140—
생성물2-(6-Methylpyridin-2-yl)ethyl methanesulfonateHCID 87885158—

반응 조건

온도0 °C

반응 단계

MsCl (6.7 mmol, 0.52 mL) was added to a solution of 6-methyl-2-pyridineethanol (6.7 mmol, 0.92 g) and triethyl amine (13.4 mmol, 1.88 mL) in toluene (6 mL) at 0° C. dropwise. The resulting mixture was stirred at 0° C. for 30 min. The precipitate generated from reaction was filtered off. The filtrate was concentrated in vacuo to give crude 2-(6-methylpyridin-2-yl)ethyl methanesulfonate which was used for next step without further purification. A mixture of above described 2-(6-methylpyridin-2-yl)ethyl methanesulfonate, PhOH (13.4 mmol, 1.26 g) and NaOH (13.4 mmol, 0.54 g) in isopropanol (20 mL) was refluxed at 90° C. for 3 h. The reaction mixture was concentrated in vacuo and dissolved in EtOAc which was washed with water. The organic layer was separated, dried with MgSO4 and concentrated in vacuo. The crude product was purified by chromatography to give desired 2-methyl-6-(2-phenoxyethyl)pyridine as a colorless oil in 26% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440982B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-5815eb26c1a244d6995a88f54424a4fe
출처 메모uspto-grants-2016_09