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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1452796생성일: 2026년 10월 25일

ethyl (2Z)-3-iodoprop-2-enoate → 5-(4-Methylsulfanyl-phenyl)-pent-2-en-4-ynoic acid ethyl ester

https://huagongshe.com/reaction/1452796

반응식

참여 물질

역할이름HCID투입량
반응물ethyl (2Z)-3-iodoprop-2-enoateHCID 643843—
반응물1-Ethynyl-4-(methylsulfanyl)benzeneHCID 6432548—
생성물5-(4-Methylsulfanyl-phenyl)-pent-2-en-4-ynoic acid ethyl esterHCID 76556503—

반응 단계

The general procedure was used to convert 1-Ethynyl-4-methylsulfanyl-benzene and (Z)-ethyl-3-iodoacrylate to the title product. Purification by flash chromatography (20% ethyl acetate in hexane as the eluent) gave the analytically pure product as a light yellow oil (450 mg, 91% yield). 1H NMR (400 MHz, CDCl3) δ 7.44-7.42 (d, J=8.5, 2H), 7.18-7.16 (d, J=8.5, 2H), 6.35-6.32 (d, J=11.4, 1H), 6.11-6.09 (d, J=11.4, 1H), 4.28-4.22 (q, J=7.1, 2H), 2.46 (s, 3H), 1.34-1.30 (t, J=7.1, 3H). 13C NMR (100 MHz, CDCl3) δ 164.81, 140.87, 132.33, 127.85, 125.68, 122.81, 118.84, 101.21, 86.77, 60.37, 15.16, 14.32. Anal. Calcd. for C14H14O2S: C, 68.26; H, 5.73; S, 13.02; Found C, 68.50; H, 5.88; S, 13.18.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07473797B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-d452962cb6a24878bf83342120789980
출처 메모uspto-grants-2009_01