反応式
[C:1]1([C:7]#[C:8][CH2:9]O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S([Cl:21])(C1C=CC(C)=CC=1)(=O)=O>N1C=CC=CC=1>[C:1]1([C:7]#[C:8][CH2:9][Cl:21])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
4
実験手順
1-Phenyl-1-propyn-3-ol (5 g), 5.1 g of tosyl chloride and 20 ml of pyridine were stirred at room temperature for 1 hour. The reaction mixture was poured into 100 ml of ice water and extracted with ethyl acetate. The oil layer was washed with 1N hydrochloric acid and saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled away. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to give 2.54 g of 3-phenyl-2-propynyl chloride as a pale yellow, oily substance.
後処理
- extractionextracted with ethyl acetate
- washThe oil layer was washed with 1N hydrochloric acid and saturated brine
- dry with materialdried over anhydrous sodium sulfate
- distillationThe solvent was distilled away
- customThe residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5)
出典と根拠
- ORDレコード
- ord-2be5ba4d22d94bdcac2a7ca824c05221
- 出典データセット
- uspto-grants-1997_02
- 特許番号
- US05604229
関連ノート
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