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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15740생성일: 2026년 10월 24일

Toluene → Ethyl 1-(4-chlorophenylsulfonyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylate

https://huagongshe.com/ko/reaction/15740

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Ethyl oxoacetateHCID 70211—
반응물4-Chlorobenzenesulfonyl isocyanateHCID 138587—
반응물1-Methoxy-3-trimethylsilyl-1,3-butadieneHCID 86613460—
생성물Ethyl 1-(4-chlorophenylsulfonyl)-4-oxo-1,2,3,4-tetrahydropyridine-2-carboxylateHCID 5934238334%

반응 단계

A solution of ethyl glyoxalate (27 mL, 0.14 mol) and 4-chlorobenzene sulfonylisocyanate (20 mL, 0.14 mol) in toluene (300 mL) was heated at reflux for 60 hours. The reaction mixture was cooled to room temperature and 1-methoxy-3-trimethylsilyl-1,3-butadiene (27 mL, 0.14 mol) was added, The reaction was heated at 50° C. for 18 hours. The reaction mixture was concentrated in vacuo and the residue was purified by flash chromatography (20% EtOAc/hexanes) to yield 16.0 g (34%) of compound 103 as a yellow oil. 1H NMR (CDCl3) δ 7.81 (d, 2H), 7.67 (dd, 1H), 7.55 (d, 2H), 5.40 (d, 1H), 5.01-4.97 (m, 1H), 4.13-4.03 (m, 3H), 2.86-2.81 (m, 2H), 1.16 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732609B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b368fd23c59347eab5cf35ba6b8dfa43
출처 메모uspto-grants-2010_06