反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[CH:5]([Cl:7])[Cl:6].[OH-].[Na+].C(Cl)(Cl)(Cl)[Cl:14]>CCCCCCCCCCCC[N+](C)(C)C.[Cl-]>[CH3:1][C:2]1[CH:3]=[C:4]([C:5]([Cl:14])([Cl:7])[Cl:6])[CH:8]=[CH:9][CH:10]=1参加物
5
実験手順
70.0 gms of 3-methyl benzal chloride dissolved in 286.4 gms of carbon tetrachloride was charged into a reaction vessel with 2.67 gms of Aliquat 4 (dodecyltrimethylammonium chloride in alcohol). 192 gms of 50% aqueous sodium hydroxide was added and the mixture heated to reflux for a period of about 4 hours. During this period water was continuously removed from the reaction media using a Dean Stark Trap. After completion of the reaction, the mixture was filtered, water was added to the mixture, and the organic layer was separated by phase separation. The organic layer was stripped on a rotary evaporator to give 84.9 gms of a clear yellow oil. (Yield 93.4%).
後処理
- temperaturethe mixture heated
- temperatureto reflux for a period of about 4 hours
- customDuring this period water was continuously removed from the reaction media
- customAfter completion of the reaction
- filtrationthe mixture was filtered
- additionwater was added to the mixture
- customthe organic layer was separated by phase separation
- customThe organic layer was stripped on a rotary evaporator
出典と根拠
- ORDレコード
- ord-ccd16b13fb7842e7813ae4946baa47b7
- 出典データセット
- uspto-grants-1986_06
- 特許番号
- US04593144
関連ノート
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