反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH2:6][OH:7].[H-].[Na+].O([CH2:21][P:22]([O:27][CH2:28][CH3:29])([O:24][CH2:25][CH3:26])=[O:23])S(C(F)(F)F)(=O)=O>CN(C=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:6][O:7][CH2:21][P:22](=[O:23])([O:27][CH2:28][CH3:29])[O:24][CH2:25][CH3:26])[CH:8]=[CH:9][CH:10]=1参加物
5
実験手順
A mixture of 3-methoxybenzyl alcohol (1 mmol) and sodium hydride (1.5 mmol) in 5 mL DMF was stirred at rt for 1 h and then added via cannula to a solution of diethylphosphonomethyl triflate (1 mmol) in 5 mL of DMF and the resulting mixture stirred at rt for 16 h. Extraction and chromatography provided diethyl 3-methoxyphenylmethoxymethylphosphonate as an oil.
後処理
- stirringthe resulting mixture stirred at rt for 16 h
- extractionExtraction and chromatography
出典と根拠
- ORDレコード
- ord-29d8e591a7e847ed847aece255246ad8
- 出典データセット
- uspto-grants-2008_05
- 特許番号
- US07371739B2
関連ノート
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