Ethylene Glycol → 1,4-Dioxaspiro[4.5]decan-8-ylmethanol

HRID 1363721Notes

Reaction equation

HRID 1363721 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]1

Participants

5

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

  1. temperaturewas heated
  2. temperatureAfter cooling the solution
  3. washwas washed with sodium bicarbonate solution
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated
  6. additionlithium aluminium hydride (7 g) was added
  7. additionwater (20 mL), 10% sodium hydroxide (30 mL) and water (30 mL) was added carefully
  8. additionSodium sulphate (30 g) was then added
  9. stirringthe mixture stirred for 20 min
  10. customThe insoluble material was removed by filtration
  11. 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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