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Hydrochloric Acid → 5-Benzyl-2-hydroxy-benzaldehyde

HRID 2057955
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2057955
[OH-:1].[Na+].[CH2:3]([C:10]1[CH:15]=[CH:14][C:13]([OH:16])=[CH:12][CH:11]=1)[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH:17](Cl)(Cl)Cl.Cl>C(O)C.O>[CH2:3]([C:10]1[CH:11]=[C:12]([CH:17]=[O:1])[C:13]([OH:16])=[CH:14][CH:15]=1)[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 6212Chloroform2×HCID 75634-BenzylphenolHCID 14798Sodium Hydroxide

Produkt 1

HCID 45126705-Benzyl-2-hydroxy-benzaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittel
HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
75 °C

Versuchsvorschrift

157 g of sodium hydroxide (50% in water) was added all at once to a stirred mixture of 100 g of p-benzylphenol in 165 ml of ethanol. The mixture was heated to 75°-80° C., and 161.5 g of chloroform was added drop-by-drop to the stirred mixture over a 5-hour period, at 75°-80° C., then was stirred for 2 hours at 75° C. Then 80.8 g of chloroform was added drop-by-drop, at 75°-80° C., and the mixture was stirred for 1 hour at 75° C. This procedure was repeated. The mixture was concentrated under reduced pressure to give a solid residue. The residue was poured into water, and the stirred mixture was acidified with concentrated hydrochloric acid. The aqueous phase was separated, extracted with ether and the extract was concentrated under reduced pressure to give an oil. The oil was extracted with petroleum ether. The extract was concentrated under reduced pressure. The residue was suspended in 150 ml of a saturated solution of sodium bisulfite and the mixture was stirred for 1 hour at room temperature. The liquid was decanted, and the solid was washed with water, stirred with ethanol and the mixture was filtered. The solid was washed with ether, then suspended in 10% sulfuric acid solution. The resulting mixture was stirred for 11/2 hours, then extracted with ether. The extract was dried (MgSO4) and concentrated under reduced pressure to give 5-benzylsalicylaldehyde (1A).

Aufarbeitung

  1. temperatureThe mixture was heated to 75°-80° C.
  2. stirringthe mixture was stirred for 1 hour at 75° C
  3. concentrationThe mixture was concentrated under reduced pressure
  4. customto give a solid residue
  5. customThe aqueous phase was separated
  6. extractionextracted with ether
  7. concentrationthe extract was concentrated under reduced pressure
  8. customto give an oil
  9. extractionThe oil was extracted with petroleum ether
  10. concentrationThe extract was concentrated under reduced pressure
  11. stirringthe mixture was stirred for 1 hour at room temperature
  12. customThe liquid was decanted
  13. washthe solid was washed with water
  14. stirringstirred with ethanol
  15. filtrationthe mixture was filtered
  16. washThe solid was washed with ether
  17. stirringThe resulting mixture was stirred for 11/2 hours
  18. extractionextracted with ether
  19. dry with materialThe extract was dried (MgSO4)
  20. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-2b500a1084364936b6316fdaa053a0b8
Quelldatensatz
uspto-grants-1980_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04213999

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