ethyl (2Z)-3-iodoprop-2-enoate → 5-(4-Vinyl-phenyl)-pent-2-en-4-ynoic acid ethyl ester
반응식
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH2:10])=[CH:5][CH:4]=1)#[CH:2].[CH2:11]([O:13][C:14](=[O:18])/[CH:15]=[CH:16]\I)[CH3:12]>>[CH2:11]([O:13][C:14](=[O:18])[CH:15]=[CH:16][C:2]#[C:1][C:3]1[CH:8]=[CH:7][C:6]([CH:9]=[CH2:10])=[CH:5][CH:4]=1)[CH3:12]참가 물질
3
실험 절차
The general procedure was used to convert 1-Ethynyl-4-vinyl-benzene and (Z)-ethyl-3-iodoacrylate to the title product. Purification by flash chromatography (10% ethyl acetate in hexane as the eluent) gave the analytically pure product as a light yellow oil (420 mg, 95% yield). 1H NMR (400 MHz, CDCl3) δ 7.51-7.49 (d, J=8.3, 2H), 7.39-7.37 (d, J=8.3, 2H), 6.73-6.66 (dd, J=17.5, 10.8, 1H), 6.38-6.35 (d, J=11.4, 1H), 6.14-6.12 (d, J=11.4, 1H), 5.81-5.77 (d, J=17.6, 1H), 5.33-5.30 (d, J=10.9, 1H), 4.29-4.24 (q, J=7.1, 2H), 1.35-1.32 (t, J=7.1, 3H). 13C NMR (100 MHz, CDCl3) δ 164.92, 139.62, 132.12, 129.28, 127.83, 123.14, 119.76, 101.77, 86.19, 60.44, 21.66, 14.42. Anal. Calcd. for C14H14O2: C, 79.62; H, 6.24; Found C, 79.37; H, 6.48.
출처 및 근거
- ORD 기록
- ord-628f2be5302e4d2e896e56473f94431b
- 출처 데이터셋
- uspto-grants-2009_01
- 특허 번호
- US07473797B2
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