Sodium Hydroxide → 2-(Benzyloxy)propanoic acid

HRID 512809

Reaktionsgleichung

Reaktionsgleichung von HRID 512809
[CH2:1]([O:8][CH:9]([CH3:14])[C:10]([O:12]C)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>O>[CH2:1]([O:8][CH:9]([CH3:14])[C:10]([OH:12])=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Komponenten

4

Reaktionsbedingungen

Temperatur
2.5 °C

Versuchsvorschrift

A mixture of residue containing methyl 2-(benzyloxy)propanoate compound of formula-12 obtained in step-a) and water (500 ml) was cooled to 0-5° C. A solution of sodium hydroxide (51.5 g) in water (375 ml) was added to reaction mixture at 0-5° C. and stirred the reaction mixture for 1 hour at the same temperature. Temperature of the reaction mixture was raised to 25-30° C. and stirred for 4 hours at this temperature. After completion of the reaction, washed the reaction mixture with dichloromethane. Both dichloromethane and aqueous layers were separated and pH of aqueous layer was adjusted to 2.5 using 50% hydrochloric acid solution. Extracted the aqueous layer with dichloromethane. Distilled off the solvent from dichloromethane layer under reduced pressure to get the title compound as a residue. The obtained residue can be taken into next step without isolation.

Aufarbeitung

  1. additionA mixture of residue
  2. temperatureTemperature of the reaction mixture was raised to 25-30° C.
  3. stirringstirred for 4 hours at this temperature
  4. customAfter completion of the reaction
  5. washwashed the reaction mixture with dichloromethane
  6. customBoth dichloromethane and aqueous layers were separated
  7. extractionExtracted the aqueous layer with dichloromethane
  8. distillationDistilled off the solvent from dichloromethane layer under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-eb8e461d935e40faaf55fbea3460a006
Quelldatensatz
uspto-grants-2015_08
Patentnummer
US09102664B2

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