反応式
[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[OH:9].[H-].[Na+].S(O[CH2:23][CH:24]1[CH2:29][CH2:28][CH:27]=[CH:26][O:25]1)(C1C=CC(C)=CC=1)(=O)=O.C(=O)(O)[O-].[Na+]>CN(C)C=O>[Cl:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[O:9][CH2:23][CH:24]1[CH2:29][CH2:28][CH:27]=[CH:26][O:25]1参加物
実験手順
A solution of 359 mg of 2,4-dichlorophenol in 3 ml of dimethylformamide was stirred with 96 mg of 55% sodium hydride at room temperature for 30 minutes. A solution of 536 mg of 2-tosyloxymethyl-3,4-dihydro-2H-pyran in 2 ml of dimethylformamide was then added, and the mixture was heated at 80°-90° C. for 2 hours. The reaction mixture was then cooled and poured onto a mixture of ice and sodium bicarbonate. The mixture was extracted with diethyl ether and the extract was dried over anhydrous potassium carbonate. After evaporation of the solvent, the residue was purified by column chromatography through silica gel eluted with a 1:2 by volume mixture of benzene and hexane, to give 394 mg of 2-(2,4-dichlorophenoxymethyl)-3,4-dihydro-2H-pyran.
後処理
- temperaturethe mixture was heated at 80°-90° C. for 2 hours
- temperatureThe reaction mixture was then cooled
- extractionThe mixture was extracted with diethyl ether
- dry with materialthe extract was dried over anhydrous potassium carbonate
- customAfter evaporation of the solvent
- customthe residue was purified by column chromatography through silica gel
- washeluted with a 1:2 by volume mixture of benzene and hexane
出典と根拠
- ORDレコード
- ord-b01f641e3ceb4fab9f08a7507462b0d4
- 出典データセット
- uspto-grants-1983_12
- 特許番号
- US04421758
関連ノート
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