Malic Acid → HCID 88789569, compound

HRID 1703519Notes

Reaction equation

HRID 1703519 reaction equation
[C:1]([OH:9])(=[O:8])[CH:2]([CH2:4][C:5]([OH:7])=[O:6])[OH:3].C(=O)([O-])[O-].[K+:14].[K+]>O>[OH2:3].[C:1]([O-:9])(=[O:8])[CH:2]([CH2:4][C:5]([OH:7])=[O:6])[OH:3].[K+:14]

Participants

4

Conditions

Temperature
10 °C

Procedure

26.8 g (0.2 mole) of DL-malic acid and 13.8 g (0.1 mole) of potassium carbonate are dissolved in 200 ml of water. The solution (pH 4.1) is concentrated under reduced pressure to make the total weight thereof 60 g. The concentrated solution is cooled to 10° C., and the mixture obtained (i.e., the mixture of the concentrated solution and crystals precipitated) is stirred at the same temperature for 4 hours. After stirring, the mixture had a pH of 4.1. The crystalline precipitates are collected by filtration, washed with an aqueous 80% methanol solution, and dried at 35° C. for 16 hours. 26.4 g of monopotassium DL-malate monohydrate are obtained as crystals. The amounts of DL-malic acid, potassium and water contained in the product are shown in Table 6. The results of this table indicate that the product obtained is the pure crystals of monopotassium DL-malate monohydrate.

Workup

  1. concentrationThe solution (pH 4.1) is concentrated under reduced pressure
  2. customthe mixture obtained (i.e.
  3. additionthe mixture of the concentrated solution and crystals
  4. customprecipitated)
  5. stirringAfter stirring
  6. customThe crystalline precipitates
  7. filtrationare collected by filtration
  8. washwashed with an aqueous 80% methanol solution
  9. customdried at 35° C. for 16 hours

Sources & evidence

ORD record
ord-cc7bd885a5224710b4c8c55b882d3300
Source dataset
uspto-grants-1978_11
Patent number
US04124636

Reaction notes

Loading…