反応式
C(Cl)(=O)C(Cl)=O.CS(C)=O.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][CH2:20][OH:21])=[CH:14][CH:13]=1.C(N(CC)CC)C>ClCCl.O>[Cl:11][C:12]1[CH:13]=[CH:14][C:15]([CH2:18][CH2:19][CH:20]=[O:21])=[CH:16][CH:17]=1参加物
実験手順
To a stirred solution of oxalyl chloride (2.04 ml) in dichloromethane (40 ml) at −78° C. was added dimethyl sulphoxide (3.33 ml), and the reaction stirred for 10 min. 3-(4-Chlorophenyl)propanol (2.0 g) in dichloromethane (20 ml) was added and the reaction stirred at −78° C. for 75 min. Triethylamine (11.53 ml) was added, the reaction allowed to warm to room temperature, and stirred for 30 min. Water (150 ml) was added, and the reaction extracted with dichloromethane (2×100 ml). The combined organic extracts were washed with water (3×100 ml), dried over magnesium sulphate (2 g), and the solvent removed in vacuo to yield a yellow oil. This was purified by flash chromatography (silica, eluent dichloromethane) to yield the title compound as a pale yellow oil (0.96 g).
後処理
- stirringthe reaction stirred at −78° C. for 75 min
- stirringstirred for 30 min
- extractionthe reaction extracted with dichloromethane (2×100 ml)
- washThe combined organic extracts were washed with water (3×100 ml)
- dry with materialdried over magnesium sulphate (2 g)
- customthe solvent removed in vacuo
- customto yield a yellow oil
- customThis was purified by flash chromatography (silica, eluent dichloromethane)
出典と根拠
- ORDレコード
- ord-388446210e0c47deb6ffb08b53ee68f6
- 出典データセット
- uspto-grants-2002_10
- 特許番号
- US06462042B1
関連ノート
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