Hydrochloric Acid → HCID 178527051, Verbindung

HRID 377175

Reaktionsgleichung

Reaktionsgleichung von HRID 377175
C([O:3][P:4](Cl)[O:5]CC)C.[CH2:9]([Mg]Cl)[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.O.Cl>C(OCC)C>[CH2:9]([PH:4](=[O:3])[OH:5])[CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Komponenten

6

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

Diethylchlorophosphite (15.6 g,0.1 mol) in 100 mL of dry diethyl ether was cooled to 5° C. under an atmosphere of nitrogen. Phenethylmagnesium chloride (100 mL, 0.1 mol, 1.0 M in THF) was added dropwise over 2 hours while maintaining a temperature between 0-10° C. A thick white slurry formed and stirred at room temperature overnight. The mixture was filtered under a nitrogen atmosphere and the filtrate evaporated under reduced pressure to give a clear and colorless liquid. The liquid was stirred as 15 mL of water was added followed by 0.5 mL of concentrated hydrochloric acid. An exothermic reaction was observed and stirring continued for 15 minutes followed by extraction with ethyl acetate. The organics were combined, washed with brine, dried (MgSO4) and evaporated. The clear liquid was brought up in sodium hydroxide (40 mL, 2.0 M NaOH), stirred for 1 hour and washed once with diethyl ether. The aqueous layer was acidified to pH 1.0 with concentrated hydrochloric acid and extracted with ethyl acetate. The organics were combined, dried (MgSo4) and evaporated to give phenethylphosphinic acid (1,R=CH2CH2Ph, R1=H)(9.8 g, 58%) as a clear light yellow oil.

Aufarbeitung

  1. customA thick white slurry formed
  2. filtrationThe mixture was filtered under a nitrogen atmosphere
  3. customthe filtrate evaporated under reduced pressure
  4. customto give a clear and colorless liquid
  5. additionwas added
  6. customAn exothermic reaction
  7. stirringstirring
  8. waitcontinued for 15 minutes
  9. extractionfollowed by extraction with ethyl acetate
  10. washwashed with brine
  11. dry with materialdried (MgSO4)
  12. customevaporated
  13. stirringstirred for 1 hour
  14. washwashed once with diethyl ether
  15. extractionextracted with ethyl acetate
  16. customdried (MgSo4)
  17. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-534f9bb00fb84713bdce7359d08aada1
Quelldatensatz
uspto-grants-2000_02
Patentnummer
US06025344

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