Hydrochloric Acid → 3-[3-(Trifluoromethyl)phenoxy]propanoic acid

HRID 391354Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 391354
[H-].[Na+].[OH:3][C:4]1[CH:5]=[C:6]([C:10]([F:13])([F:12])[F:11])[CH:7]=[CH:8][CH:9]=1.[C:14]1(=[O:18])[O:17][CH2:16][CH2:15]1.Cl>O.CN(C)C=O>[F:13][C:10]([F:11])([F:12])[C:6]1[CH:5]=[C:4]([CH:9]=[CH:8][CH:7]=1)[O:3][CH2:16][CH2:15][C:14]([OH:18])=[O:17]

Komponenten

7

Versuchsvorschrift

Sodium hydride (550 mg) was added to an N,N-dimethylformamide (20.0 mL) solution of 3-hydroxybenzotrifluoride (2.0 g), and the reaction mixture was stirred at room temperature for one hour. β-Propiolactone (1.0 mL) was added thereto, and the solution was stirred at room temperature for 2.5 hours. Water was then added to the solution, and the pH was adjusted to 2 with 2 N hydrochloric acid. The solution was extracted with ethyl acetate. The organic layer was sequentially washed with water and a saturated brine and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and n-hexane was then added to the residue to perform crystallization. The title compound (2.2 g) was obtained as colorless crystals.

Aufarbeitung

  1. stirringthe solution was stirred at room temperature for 2.5 hours
  2. extractionThe solution was extracted with ethyl acetate
  3. washThe organic layer was sequentially washed with water
  4. dry with materiala saturated brine and then dried over anhydrous sodium sulfate
  5. distillationThe solvent was distilled off under reduced pressure, and n-hexane
  6. additionwas then added to the residue
  7. customcrystallization

Quellen und Nachweise

ORD-Eintrag
ord-59642f11c649458e83ef1e27c0ed5c02
Quelldatensatz
uspto-grants-2013_02
Patentnummer
US08383839B2

Notizen zur Reaktion

Wird geladen…