HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262350Generated: October 25, 2026
3-Chloro-2-methyl-1-propene → alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol
https://huagongshe.com/reaction/262350
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-2-methyl-1-propene | HCID 11241 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(3,3-Dimethylbicyclo(2.2.1)hept-5-en-2-yl)ethan-1-one | HCID 162511 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | alpha-Methallyl-alpha,3,3-trimethyl-5-norbornene-2-methanol | HCID 21319801 | 106.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04153811 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-c30ecacf408e47818c3db7040e96b44a |
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| Source note | uspto-grants-1979_05 |
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