Methanol → 2,2-dimethoxycyclopentanol

HRID 968331Notes

Reaction equation

HRID 968331 reaction equation
[C:1]1(=[O:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-:7].[K+].I(C1C=CC=CC=1[C:13](O)=[O:14])=O.[CH3:20]O>>[CH3:20][O:6][C:1]1([O:14][CH3:13])[CH2:5][CH2:4][CH2:3][CH:2]1[OH:7]

Participants

5

Conditions

Temperature
0 °C

Procedure

A solution of cyclopentanone (11.6 ml, 130 mmol) in methanol (250 ml) was added drop-wise at 0° C. over 20 minutes to a stirred solution of potassium hydroxide (85% tech., 22.1 g, 335 mmol) in methanol (75 ml). The mixture was stirred at 0° C. for 30 minutes then 2-iodosylbenzoic acid (36.45 g, 138 mmol) was added in portions over 1 hour. The mixture was allowed to warm to ambient temperature over 4 hours, then stirred at ambient temperature for 20 hours. The majority of solvent was removed in vacuo then the product was extracted into dichloromethane (400 ml), then the extracts were washed with water (2×250 ml), dried (Na2SO4) and the solvent removed in vacuo to leave 2,2-dimethoxycyclopentanol as a colourless oil (11.98 g) which was used without further purification.

Workup

  1. temperatureto warm to ambient temperature over 4 hours
  2. stirringstirred at ambient temperature for 20 hours
  3. customThe majority of solvent was removed in vacuo
  4. extractionthe product was extracted into dichloromethane (400 ml)
  5. washthe extracts were washed with water (2×250 ml)
  6. dry with materialdried (Na2SO4)
  7. customthe solvent removed in vacuo

Sources & evidence

ORD record
ord-fed4bc15d2084c0c9a084e4bca07cf0d
Source dataset
uspto-grants-2005_10
Patent number
US06958358B2

Reaction notes

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