Ethylene Glycol → 1,4-Dioxaspiro[4.5]decan-8-ylmethanol
Reaction equation
[C:1](CC1CCC(=O)CC1)(O)=[O:2].[CH2:12]([OH:15])[CH2:13][OH:14].[CH:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>O>[O:14]1[C:16]2([CH2:21][CH2:20][CH:19]([CH2:1][OH:2])[CH2:18][CH2:17]2)[O:15][CH2:12][CH2:13]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-carboxymethylcyclohexanone (21 g), ethylene glycol (19 g) and benzene (250 mL) was heated at reflux for 20 h with Dean Stark azeotropic removal of water. After cooling the solution was washed with sodium bicarbonate solution, dried over magnesium sulphate and concentrated. The crude ketal was then taken up in diethyl ether (250 mL) and lithium aluminium hydride (7 g) was added. The mixture was stirred overnight and then water (20 mL), 10% sodium hydroxide (30 mL) and water (30 mL) was added carefully. Sodium sulphate (30 g) was then added and the mixture stirred for 20 min. The insoluble material was removed by filtration and the organic phase concentrated in vacuo to give (1,4-dioxaspiro[4.5]dec-8-yl)-methanol (21 g).
Workup
- temperaturewas heated
- temperatureAfter cooling the solution
- washwas washed with sodium bicarbonate solution
- dry with materialdried over magnesium sulphate
- concentrationconcentrated
- additionlithium aluminium hydride (7 g) was added
- additionwater (20 mL), 10% sodium hydroxide (30 mL) and water (30 mL) was added carefully
- additionSodium sulphate (30 g) was then added
- stirringthe mixture stirred for 20 min
- customThe insoluble material was removed by filtration
- concentrationthe organic phase concentrated in vacuo
Sources & evidence
- ORD record
- ord-56d445f9211244a0924e4c9285dab760
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07884210B2
Reaction notes
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