Hydrochloric Acid → HCID 11984309, compound

HRID 493463Notes

Reaction equation

HRID 493463 reaction equation
[OH-].[Na+].CO.[CH3:5][C@@H:6]([CH:11]([C:17]([O:19]CC)=[O:18])[C:12]([O:14]CC)=[O:13])[CH2:7][CH2:8][CH2:9][CH3:10].Cl>O.CCOCC>[CH3:5][C@@H:6]([CH:11]([C:17]([OH:19])=[O:18])[C:12]([OH:14])=[O:13])[CH2:7][CH2:8][CH2:9][CH3:10]

Participants

7

Conditions

Temperature
70 °C

Procedure

At room temperature, 81 g of sodium hydroxide (2 mol) were dissolved in 360 ml of water and 160 ml of methanol in a three-neck flask with internal thermometer, dropping funnel and stirrer. 124 g of diethyl [(R)-1-methylpentyl]malonate (0.51 mol) were then added. The mixture was heated to 70° C. and stirred at this temperature for 3.5 h, in the course of which a solid formed. After cooling to 25° C., the suspension was admixed with 250 ml of ether and, with cooling, with 400 ml of 20% by weight hydrochloric acid. After phase separation, the aqueous phase was extracted twice with 100 ml of ether. The combined organic phases were washed with 100 ml of water and then dried over sodium sulfate. After solvent had been distilled off, [(R)-1-methylpentyl]malonic acid was obtained in a yield of 85 g (89% of theory) (m.p.: 123° C.).

Workup

  1. customformed
  2. temperatureAfter cooling to 25° C.
  3. customAfter phase separation
  4. extractionthe aqueous phase was extracted twice with 100 ml of ether
  5. washThe combined organic phases were washed with 100 ml of water
  6. dry with materialdried over sodium sulfate
  7. distillationAfter solvent had been distilled off

Sources & evidence

ORD record
ord-d99f797bfdbf4b60bf9cf2502077d058
Source dataset
uspto-grants-2009_05
Patent number
US07534908B2

Reaction notes

Loading…