Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224247Generated: October 25, 2026

Sulfuric Acid → 3-Isopropyl-1-methyl-2-oxabicyclo[2.2.2]octane

https://huagongshe.com/reaction/224247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-ChloropropaneHCID 6361—
Reactant3-Cyclohexene-1-carboxaldehyde, 4-methyl-HCID 111012—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product3-Isopropyl-1-methyl-2-oxabicyclo[2.2.2]octaneHCID 2056155689.7%
ProductHCID 178418918HCID 178418918—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of isopropyl magnesium chloride in ether is prepared by dropwise adding a solution of 410 grams (3.45 moles) of isopropyl chloride in 700 ml of dry ether to a stirred slurry of 76.5 grams of magnesium (3.15 moles) in 600 ml of dry ether under nitrogen at reflux. The resulting solution is stirred at reflux for 30 minutes. A solution of 372 grams of 4-methyl-3-cyclohexenecarboxaldehyde (3.38 moles) in 200 ml of ether is then added to the reaction mixture over a period of 1 hour at reflux under nitrogen. The resulting slurry is heated at reflux for 30 minutes and then cooled to 0° C. 1200 grams of 20% sulfuric acid is slowly added with external cooling over a 30 minute period. After the addition is complete, two clear layers appear. A distillation head is placed on the flask ether is distilled from the reaction mixture at atmospheric pressure to a pot temperature of 90° C. 500 ml of water and 300 ml of isopropyl alcohol is added to the reaction mixture. Sulfuric acid (200 grams) is added slowly and the resulting solution is heated to reflux for 9 hours. At the end of this period the reaction mass is cooled. 500 ml of water and 200 ml of toluene is added thereto with stirring. The phases are allowed to separate and the aqueous phase is discarded. The organic phase is washed twice with H2O, with sufficient sodium carbonate added to the second wash to adjust to pH to 7-8. Distillation of the organic layer affords 255 grams of 3-isopropyl-1-methyl-2-oxabicyclo[2.2.2]octane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04231940
Source datasetuspto-grants-1980_11
ORD IDord-1e42f3e436ea4820817f551102c54614
Source noteuspto-grants-1980_11