反応式
[CH2:1]([OH:5])[CH2:2][CH2:3][OH:4].CC([O-])(C)C.[K+].[F:12][C:13]1[CH:18]=[C:17]([F:19])[C:16]([F:20])=[CH:15][C:14]=1F.[Cl-].[Na+]>O.C1(C)C=CC=CC=1.CS(C)=O>[F:12][C:13]1[CH:18]=[C:17]([F:19])[C:16]([F:20])=[CH:15][C:14]=1[O:4][CH2:3][CH2:2][CH2:1][OH:5]参加物
8
実験手順
To a mixture of 1,3-propanediol (15 g, 0.20 mol) and t-BuOK (8.0 g, 0.071 mol) were added 1,2,4,5-tetrafluorobenzene (5.0 g, 33 mol) and DMSO (50 g) at 60° C. After being stirred at this temperature for 18 h, toluene (200 mL), water (50 mL) and sodium chloride (10 g) were added to the reaction mixture. The layers were separated and the organic layer was concentrated in vacuo to the title compound that was used directly in the next step.
後処理
- customThe layers were separated
- concentrationthe organic layer was concentrated in vacuo to the title compound that
出典と根拠
- ORDレコード
- ord-04fab01c7dfb40d0b7ee845903b92f4c
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07244722B2
関連ノート
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