Sodium Carbonate → 4-Methyl-3-formyl-pent-3-en-1-oic acid

HRID 615715Notes

Reaction equation

HRID 615715 reaction equation
[N+]([C:4]([CH:7]1[CH:11]([O:12]C)[O:10][C:9](=[O:14])[CH2:8]1)([CH3:6])[CH3:5])([O-])=O.C(=O)([O-])[O-].[Na+].[Na+]>CO.O>[CH:11]([C:7](=[C:4]([CH3:6])[CH3:5])[CH2:8][C:9]([OH:14])=[O:10])=[O:12]

Participants

5

Conditions

Temperature
0 °C

Procedure

A solution of 18.2 g of the product of Step A in 25 ml of methanol were added all at once to a solution of 18.9 g of sodium carbonate in 180 ml of water cooled to 0° C. and the mixture stood at room temperature for 120 hours. The mixture was washed with ether and cooled to 0° C. after which concentrated sulfuric acid was added to the mixture under an inert atmosphere until the pH was ≅1. The mixture was extracted with chloroform and then with ethyl acetate and the combined organic phases were dried and evaporated to dryness under reduced pressure to obtain 9.5 g of residue. The latter was crystallized from water to obtain 7.4 g of pure 3-formyl-4-methyl-pent-3-one-1-oic acid melting at 102° C.

Workup

  1. washThe mixture was washed with ether
  2. temperaturecooled to 0° C. after which concentrated sulfuric acid
  3. additionwas added to the mixture under an inert atmosphere until the pH
  4. extractionThe mixture was extracted with chloroform
  5. dry with materialwith ethyl acetate and the combined organic phases were dried
  6. customevaporated to dryness under reduced pressure

Sources & evidence

ORD record
ord-15b14b64e89a4fb7999f30a6602d68be
Source dataset
uspto-grants-1985_02
Patent number
US04500720

Reaction notes

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