反応式
[C:1]1([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][CH:8]([CH2:12][CH3:13])[C:9](O)=[O:10].S(Cl)([Cl:22])=O>>[C:1]1([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][CH:8]([CH2:12][CH3:13])[C:9]([Cl:22])=[O:10]参加物
3
実験手順
To a 100-ml three-necked round flask (equipped with stirrer chip, Dimroth condenser, thermometer and NaOH trap) were introduced 13.3 g (52.4 mmol) of the 3-(2-biphenylyl)-2-ethylpropionic acid and 25.9 ml (355 mmol) of thionyl chloride, and they were refluxed for 2.5 hours with heating in a nitrogen atmosphere. After the reaction was completed, the unreacted thionyl chloride was distilled off under reduced pressure to obtain 15.2 g of a crude product of yellow orange liquid. This acid chloride was used for the next reaction without further purification. The properties of the product thus obtained are described below.
後処理
- customTo a 100-ml three-necked round flask (equipped with stirrer chip, Dimroth condenser
- temperaturewere refluxed for 2.5 hours
- temperaturewith heating in a nitrogen atmosphere
- distillationthe unreacted thionyl chloride was distilled off under reduced pressure
出典と根拠
- ORDレコード
- ord-ca9642abf1f94eaca83a79f5b40c43cb
- 出典データセット
- uspto-grants-1997_10
- 特許番号
- US05677408
関連ノート
読み込み中…