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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 262073Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/262073

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Chloro-2-methyl-1-propeneHCID 11241—
EduktAmmonium ChlorideHCID 25517—
Edukt1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-oneHCID 162511—
EduktMagnesiumHCID 5462224—
LösungsmittelDiethyl EtherHCID 3283—
Produktalpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanolHCID 21319801106,5%

Reaktionsschritte

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®.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04153568
Quelldatensatzuspto-grants-1979_05
ORD IDord-fcd3a452c59e434ea142376aea1dad83
Quellennotizuspto-grants-1979_05