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Under nitrogen, 2.211 g NaH was suspended in 50 mL dry ether in a three-necked round bottom flask. Anhydrous (CH3)2SO (5.0 mL) was added. The flask was cooled with ice. 2,2-Dimethyl-4-penten-1-ol (7.0 g) in 13 mL anhydrous ether was added dropwise through an addition funnel. The solution was then refluxed overnight. Upon cooling in ice, 43.56 g CH3I (5 eq) was added through an addition funnel. Soon a white precipitate was seen. The slurry was refluxed for 4 h. Upon cooling, water and ether were added to the mixture. The ether layer was separated, washed with water twice and dried with Na2SO4. Careful evaporation of ether (the product has a low b.p.) gave 2.0 g pure product. 1H NMR(CDCl3): δ0.86(s, 6H, —CMe2—); 2.00.(d, 2H, CH2═CH—CH2—); 3.05(s, 2H, , —CH2OMe); 3.33(s, 3H, —CH2OMe); 5.00(m, 2H, CH2═CH—); 5.80(m, 1H, CH2═CH—)

1. temperatureThe flask was cooled with ice
2. temperatureThe solution was then refluxed overnight
3. temperatureUpon cooling in ice
4. temperatureThe slurry was refluxed for 4 h
5. temperatureUpon cooling
6. customThe ether layer was separated
7. washwashed with water twice
8. dry with materialdried with Na2SO4
9. customCareful evaporation of ether (the product