Hydrochloric Acid → (2-Ethyl-1,6-dioxaspiro[4.5]decan-2-yl)methanol
Reaction equation
[CH2:1]([C:3]1([O:13][CH2:12]1)[CH2:4][CH2:5][C:6]1[O:11][CH2:10][CH2:9][CH2:8][CH:7]=1)[CH3:2].Cl.C([O:17]CC)C>O1CCCC1>[CH2:1]([C:3]1([CH2:12][OH:17])[CH2:4][CH2:5][C:6]2([CH2:7][CH2:8][CH2:9][CH2:10][O:11]2)[O:13]1)[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To 5.5 g of 6-(3-ethyl-(3,4-epoxybutyl))-3,4-dihydro-2H-pyran was added a solution of 2 ml of 10% hydrochloric acid in 25 ml of tetrahydrofuran. The reaction mixture was stirred under nitrogen for five days and then poured into 150 ml of diethyl ether. The resulting solution was washed twice with 50 ml of saturated sodium bicarbonate solution, and dried, and the solvent was removed under high vacuum to yield 6 g of the desired product as a dark brown oil.
Workup
- washThe resulting solution was washed twice with 50 ml of saturated sodium bicarbonate solution
- customdried
- customthe solvent was removed under high vacuum
Sources & evidence
- ORD record
- ord-cadce283ebfd4e47ad7d3e5fa611f4d4
- Source dataset
- uspto-grants-1983_10
- Patent number
- US04410354
Reaction notes
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