Potassium Hydroxide → 3,3-Dimethyl-1-butene
Reaction equation
[OH-:1].[K+].[OH-].[Na+].[CH2:5](Cl)[CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8]>>[CH2:5]=[CH:6][C:7]([CH3:10])([CH3:9])[CH3:8].[CH2:5]([OH:1])[CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8].[CH2:5]([O:1][CH2:5][CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8])[CH2:6][C:7]([CH3:10])([CH3:9])[CH3:8]Participants
6
Procedure
The procedure of Example 1 is followed; instead of using potassium hydroxide, 1 mole of potassium hydroxide and 1 mole of sodium hydroxide is utilized, as well as 2 moles of neohexyl chloride. A conversion of about 50% is attained in this procedure. The yields of neohexene, neohexanol, and dineohexyl ether, based on converted neohexyl chloride, are 70.0 mol-%, 6.1 mol-%, and 7.1 mol-%, respectively.
Sources & evidence
- ORD record
- ord-6fb8936451564dce8d0920781e796168
- Source dataset
- uspto-grants-1986_04
- Patent number
- US04579992
Reaction notes
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