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Hydrochloric Acid → (R)-2-(4-(benzyloxy)phenyl)-2-hydroxyacetic acid

HRID 1003278
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1003278
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([C@@H:6]([OH:10])[C:7]([OH:9])=[O:8])=[CH:4][CH:3]=1.[CH2:13](Br)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.C(=O)([O-])[O-].[K+].[K+].Cl>CN(C)C=O>[CH2:13]([O:1][C:2]1[CH:12]=[CH:11][C:5]([C@@H:6]([OH:10])[C:7]([OH:9])=[O:8])=[CH:4][CH:3]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 440639(R)-4-hydroxymandelic acid

Produkt 1

HCID 14010320(R)-2-(4-(benzyloxy)phenyl)-2-hydroxyacetic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

(R)-4-Hydroxymandelic acid (2.02 g) was dissolved in N,N-dimethylformamide (24 ml), and benzyl bromide (3.57 ml) and potassium carbonate (3.65 g) were added to the solution at room temperature with stirring. After reaction for 12 hours, ice-water was poured into the reaction mixture and the resulting precipitates were collected by filtration. The precipitates were suspended in methanol (24 ml) and 1N aqueous sodium hydroxide solution (12 ml) was added to the suspension under ice-cooling with stirring. After reaction at room temperature for 2 hours, 1N hydrochloric acid (12 ml) was added to the reaction mixture under ice-cooling with stirring. Collection by filtration of the resulting precipitates gave (R)-4-benzyloxymandelic acid (2.43 g) having a melting point of 161-163° C.

Aufarbeitung

  1. customAfter reaction for 12 hours
  2. customthe resulting precipitates
  3. filtrationwere collected by filtration
  4. addition1N aqueous sodium hydroxide solution (12 ml) was added to the suspension under ice-
  5. temperaturecooling
  6. stirringwith stirring
  7. customAfter reaction at room temperature for 2 hours
  8. temperaturecooling
  9. stirringwith stirring
  10. customCollection
  11. filtrationby filtration of the resulting
  12. customprecipitates

Quellen und Nachweise

ORD-Eintrag
ord-06f37a9b77004545a8a86416b22b334e
Quelldatensatz
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06046192

Notizen zur Reaktion

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