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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614067Generated: October 25, 2026

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

https://huagongshe.com/reaction/614067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-oneHCID 162511—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Productalpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanolHCID 21319801106.5%

Reaction Steps

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 one-half 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 one-half 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®.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04143074
Source datasetuspto-grants-1979_03
ORD IDord-a38d6262732c4b6ba9d404ebe2a9dda5
Source noteuspto-grants-1979_03