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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 497414생성일: 2026년 10월 26일

2-Methoxy-5-nitropyridine → 6-Methoxy-3-nitro-2-(toluene-4-sulfonylmethyl)-pyridine

https://huagongshe.com/reaction/497414

반응식

참여 물질

역할이름HCID투입량
반응물2-Methoxy-5-nitropyridineHCID 79525—
반응물1-Chloromethanesulfonyl-4-methylbenzeneHCID 562845—
반응물Potassium tert-butoxideHCID 23665647—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물6-Methoxy-3-nitro-2-(toluene-4-sulfonylmethyl)-pyridineHCID 1362651437.2%

반응 단계

A mixture of 15.4 g (0.1 mol) of 6-methoxy-3-nitropyridine and 20.4 g (0.1 mol) of 1-chloromethane-sulfonyl-4-methyl-benzene is dissolved in 100 mL of DMF and cooled to 5 C. To this solution is added, dropwise, 100 mL (0.1 mol) of a 1M solution of potassium t-butoxide in THF, keeping the temperature ≦10 C. The dark reaction mixture is stirred for 18 hours at room temperature. The reaction mixture is evaporated to remove the THF, and to the remaining solution is added 100 mL of water. A dark brown precipitate formed which is collected by filtration. This solid is triturated with isopropyl ether for 1 hour and refiltered to yield 12 grams of 6-methoxy-3-nitro-2-(toluene-4-sulfonylmethyl)-pyridine. 1H NMR (CDCl3) δ 8.25 (d, 1H), 7.60 (m, 2H), 7.30 (m, 2H), 6.80 (d, 1H), 5.10 (s, 1H), 3.75 (s, 3H), 2.40 (s, 3H). Mass Spectrum: m/e=323.1 (p+1), TLC (CDCl3) Rf=0.45 Step 2:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06949562B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-ee4fbb90b9de42b094f980cd6699cdcf
출처 메모uspto-grants-2005_09