Iodoethane → HCID 178476810、化合物
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][C:15]=1[N+:16]([O-:18])=[O:17])[CH2:6][CH:7]=[CH:8][CH2:9][PH:10](=[O:12])[OH:11].I[CH2:20][CH3:21].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][C:15]=1[N+:16]([O-:18])=[O:17])[CH2:6][CH:7]=[CH:8][CH2:9][PH:10](=[O:11])[O:12][CH2:20][CH3:21]参加物
実験手順
A mixture of (3-methoxy-4-nitrobenzyl)prop-2-en-1-ylphosphinic acid (Compound 37F, 1.28 g, 4.72 mmol) and iodoethane (1.47 g, 9.44 mmol) in DMF (5.0 mL) was charged with potassium carbonate (1.30 g, 9.44 mmol). The reaction mixture was allowed to stir at rt for 16 hours. The reaction mixture was quenched with water (15 mL) and extracted with EtOAc (25 mL). The organic layer was washed with water (10 mL), washed with brine (10 mL), dried over Na2SO4, filtered, concentrated under reduced pressure to yield a yellow oil. The crude material was purified on a Teledyne ISCO Combiflash® Rf system using DCM/MeOH (100:0→95:5) as eluent to afford the title compound as 1.08 g of a yellow oil (77%). 1H NMR (CDCl3, 400 MHz): δ=7.84 (d, J=8.3 Hz, 1H), 7.11 (t, J=1.8 Hz, 1H), 6.92 (td, J=1.8, 8.3 Hz, 1H), 5.76-5.90 (m, 1H), 5.18-5.32 (m, 2H), 4.00-4.14 (m, 2H), 3.98 (s, 3H), 3.19 (d, J=16.4 Hz, 2H), 2.60 (dd, J=7.3, 17.7 Hz, 2H), 1.29 (t, J=7.1 Hz, 3H). MS (ESI): m/z 300.10 [M+H]+. UPLC: tR=1.22 min (UPLC-TOF: polar—3 min).
後処理
- customThe reaction mixture was quenched with water (15 mL)
- extractionextracted with EtOAc (25 mL)
- washThe organic layer was washed with water (10 mL)
- washwashed with brine (10 mL)
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto yield a yellow oil
- customThe crude material was purified on a Teledyne ISCO Combiflash® Rf system
出典と根拠
- ORDレコード
- ord-a443cf87aea241179de57b37be55f6fc
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09133224B2
反応ノート
読み込み中…