反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5]O.C(N(CC)CC)C.S(Cl)([Cl:19])=O>C1C=CC=CC=1>[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][Cl:19]参加物
5
実験手順
3-Hydroxybenzylalcohol (5 g, 40 mmol) and triethylamine (5.2 ml, 60 mmol) were dissolved in benzene (250 ml), and thionylchloride (5.2 ml) dissolved in benzene (50 ml) was added thereto at 0° C. The brownish reacting solution was stirred at room temperature for 6 hours. When the reaction was completed, the solution was washed with brine, and the water layer was extracted with methylene chloride. The organic extract was dried over anhydrous magnesium sulfate and concentrated under a reduced pressure to obtain the title compound (5.7 g, 99%).
後処理
- additionwas added
- customat 0° C
- washthe solution was washed with brine
- extractionthe water layer was extracted with methylene chloride
- extractionThe organic extract
- dry with materialwas dried over anhydrous magnesium sulfate
- concentrationconcentrated under a reduced pressure
出典と根拠
- ORDレコード
- ord-1d9b2f92f1e840efb716f8ecf6ea906d
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07741323B2
関連ノート
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