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HRID 1112029作成日:2026年10月25日

3-Chloro-2-methyl-1-propene → alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol

https://huagongshe.com/reaction/1112029

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-2-methyl-1-propeneHCID 11241—
反応物Ammonium ChlorideHCID 25517—
反応物1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-oneHCID 162511—
反応物MagnesiumHCID 5462224—
溶媒Diethyl EtherHCID 3283—
生成物alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanolHCID 21319801106.5%

反応手順

Into a 1 liter reaction flask equipped with a reflux condenser, thermometer, stirrer, dropping funnel and nitrogen inlet tube are placed 12 g (0.5 moles) of magnesium turnings and 250 cc anhydrous diethyl ether. Over a 2 hour period, 45.3 g (0.5 moles) of methallyl chloride is added. The Grignard solution is stirred for 1/2 hour and 28 g of 2-acetyl-3,3-dimethyl-5-norbornene is added over a 20 minute period. The mixture is stirred at reflux for 1/2 hour and then is hydrolyzed by the addition of saturated ammonium chloride solution. The organic layer is washed with water and dried over magnesium sulfate. The mixture is then filtered and the solvent evaporated to yield 40 g of an oil, which is then fractionated on a micro Vigreux column after adding thereto 5 g Primol® and a trace quantity of Ionox® .

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04120308
出典データセットuspto-grants-1978_10
ORD IDord-e6b2a754b2194a85a1b7f83fd1245ec9
出典メモuspto-grants-1978_10