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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112625Generated: October 26, 2026

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

https://huagongshe.com/reaction/1112625

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 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®.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123393
Source datasetuspto-grants-1978_10
ORD IDord-3434ab00ee504ba788184907d5cecfb1
Source noteuspto-grants-1978_10