Acetic Acid → HCID 19913834, compound

HRID 1110917Notes

Reaction equation

HRID 1110917 reaction equation
[CH:1]([N-]C(C)C)(C)C.[Li+].[CH3:9][O:10][C:11](=[O:16])[CH2:12][C:13]([CH3:15])=[O:14].C[C:18]1[CH:19]=[CH:20][C:21]2[C:26](=[O:27])OC[O:23][C:22]=2[CH:28]=1.C(O)(=O)C>O1CCCC1.C(OCC)(=O)C>[OH:23][C:22]1([CH3:1])[CH:28]=[CH:18][CH:19]=[CH:20][CH:21]1[C:26](=[O:27])[CH2:15][C:13](=[O:14])[CH2:12][C:11]([O:10][CH3:9])=[O:16]

Participants

7

Procedure

To a solution of 41.6 mmol of lithium diisopropyl amide in tetrahydrofuran (formed by adding n-butyl lithium in hexanes to diisopropyl amine in THF) is added 2.4 g (20.8 mmole) of methylacetoacetate over 10 minutes at O° C. After stirring for 30 minutes, 2.0 g of 7-methyl-1,3-benzodioxane-4-one is added and the mixture stirred for 30 minutes. 6 ml of acetic acid is added and the mixture diluted with ethyl acetate and filtered The ethyl acetate solution is washed with diluted hydrochloric acid, water and dried over sodium sulfate. The ethyl acetate is removed in vacuo to give methyl 5-(2-hydroxy-2-methylphenyl)-3,5-dioxopentanoate.

Workup

  1. stirringthe mixture stirred for 30 minutes
  2. filtrationfiltered The ethyl acetate solution
  3. washis washed with diluted hydrochloric acid, water
  4. dry with materialdried over sodium sulfate
  5. customThe ethyl acetate is removed in vacuo

Sources & evidence

ORD record
ord-a69aa70ec0d64f5e9d58b1e93f860deb
Source dataset
uspto-grants-1990_12
Patent number
US04977162

Reaction notes

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