Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
ethyl (2Z)-3-iodoprop-2-enoate → 5-(4-Methylsulfanyl-phenyl)-pent-2-en-4-ynoic acid ethyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | ethyl (2Z)-3-iodoprop-2-enoate | HCID 643843 | — |
| 반응물 | 1-Ethynyl-4-(methylsulfanyl)benzene | HCID 6432548 | — |
| 생성물 | 5-(4-Methylsulfanyl-phenyl)-pent-2-en-4-ynoic acid ethyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07473797B2 |
| 출처 데이터셋 | uspto-grants-2009_01 |
| ORD ID | ord-d452962cb6a24878bf83342120789980 |
| 출처 메모 | uspto-grants-2009_01 |