Hydrochloric Acid → 5-hydroxy-5-methylhexan-2-one

HRID 1816946Notes

Reaction equation

HRID 1816946 reaction equation
[CH3:1][C:2]([OH:12])([CH2:4][CH2:5][C:6]1([CH3:11])OCC[O:7]1)[CH3:3].Cl.[OH-].[Na+]>CC(C)=O>[OH:12][C:2]([CH3:3])([CH3:1])[CH2:4][CH2:5][C:6](=[O:7])[CH3:11]

Participants

5

Procedure

The obtained 2-methyl-4-(2-methyl[1,3]dioxolan-2-yl)butan-2-ol (21.18 g) was dissolved in acetone (165 ml). Thereafter, 1 M hydrochloric acid (6.6 ml) was added to the solution, and the obtained mixture was stirred at a room temperature for 2 hours. The reaction solution was neutralized with an aqueous 1 M sodium hydroxide solution. Thereafter, a saturated saline solution (100 ml) was added thereto, and acetone was then distilled off under a reduced pressure. After extraction with chloroform (200 ml×4), the organic layer was dried over anhydrous sodium sulfate. The solvent was then eliminated under a reduced pressure to obtain 5-hydroxy-5-methylhexan-2-one (14.23 g).

Workup

  1. distillationacetone was then distilled off under a reduced pressure
  2. extractionAfter extraction with chloroform (200 ml×4)
  3. dry with materialthe organic layer was dried over anhydrous sodium sulfate

Sources & evidence

ORD record
ord-68f1967a99bd4f7289be026f4c8d9c7a
Source dataset
uspto-grants-2009_10
Patent number
US07598244B2

Reaction notes

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