戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 616064作成日:2026年10月26日

Ammonium Chloride → 4-(2,6,6-Trimethyl-2-cyclohexen-1-ylidene)-butan-2-ol

https://huagongshe.com/reaction/616064

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物Sodium borohydrideHCID 4311764—
反応物4-(2,6,6-Trimethylcyclohex-2-en-1-ylidene)but-2-en-2-yl acetateHCID 53406773—
溶媒EthanolHCID 702—
生成物4-(2,6,6-Trimethyl-2-cyclohexen-1-ylidene)-butan-2-olHCID 53692157107.2%

反応手順

The resulting crude acetoxy compound of formula II (108 g) is dissolved in 400 ml of ethanol (96%) and added dropwise within 10 minutes at 20°-30° C with slight cooling to a suspension of 20 g of sodium borohydride in 600 ml of 96% ethanol. The mixture is then heated until a slight reflux occurs and stirred at this temperature for 15 minutes. The end of the reaction can be detected by a spontaneous colour change from dark-yellow to lemon-yellow. After cooling to room temperature, the cloudy mixture is poured on to saturated ammonium chloride solution/ice and the mixture is extracted with hexane. After the usual washing to neutrality with water and drying over anhydrous sodium sulphate, the solvent is evaporated under a vacuum. There are obtained 96 g of crude 4-(2,6,6-trimethyl-2-cyclohexen-1-ylidene)-butan-2-ol (formula III).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04072719
出典データセットuspto-grants-1978_02
ORD IDord-14aeedd14fd4480ea6b33e5898f7eea6
出典メモuspto-grants-1978_02