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Hydrochloric Acid → HCID 69331765, Verbindung

HRID 1765986
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1765986
C([NH:4][C@@H:5]([C:16]([OH:18])=[O:17])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([CH3:13])=[C:9]([O:14][CH3:15])[CH:8]=1)(=O)C.C1(C)C=CC=CC=1.[ClH:26]>>[ClH:26].[CH3:15][O:14][C:9]1[CH:8]=[C:7]([CH:12]=[CH:11][C:10]=1[CH3:13])[CH2:6][C@H:5]([C:16]([OH:18])=[O:17])[NH2:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 313Hydrochloric AcidHCID 1140TolueneHCID 54030461HCID 54030461, Verbindung

Produkt 1

HCID 69331765HCID 69331765, Verbindung

Versuchsvorschrift

A mixture of N-acetyl-3-methoxy-4-methyl-D-phenylalanine (2.55 g) in a mixture of 6N hydrochloric acid (25.5 ml) with toluene (18 ml) was stirred under reflux for 4 hours. After cooling to room temperature, the aqueous layer was separated and the organic layer was washed twice with water (10 ml). The aqueous layer and the washings were combined and the solvent was evaporated under reduced pressure. The produced crystals were collected by filtration and washed with ice-water to give 3-methoxy-4-methyl-D-phenylalanine hydrochloride (1.35 g) in the form of colorless crystals. The solvent was evaporated from the filtrate under reduced pressure to give crude 3-methoxy-4-methyl-D-phenylalanine hydrochloride (0.6 g).

Aufarbeitung

  1. temperatureunder reflux for 4 hours
  2. customthe aqueous layer was separated
  3. washthe organic layer was washed twice with water (10 ml)
  4. customthe solvent was evaporated under reduced pressure
  5. filtrationThe produced crystals were collected by filtration
  6. washwashed with ice-water

Quellen und Nachweise

ORD-Eintrag
ord-0a834d6d19f44ad59a49cf9c800f5927
Quelldatensatz
uspto-grants-2007_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07229992B2

Notizen zur Reaktion

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