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Potassium Iodide → N-(2-methylphenyl)valine

HRID 648247
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 648247
Br[CH:2]([CH:20]([CH3:22])[CH3:21])[C:3]([O:5]CC1C=CC=C(OC2C=CC=CC=2)C=1)=[O:4].[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=1[NH2:26].[I-].[K+]>S(=O)(=O)(O)O>[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=1[NH:26][C@H:2]([C:3]([OH:5])=[O:4])[CH:20]([CH3:22])[CH3:21]
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Komponenten

5

Edukt 3

HCID 4875Potassium IodideHCID 7242O-ToluidineHCID 13229492m-Phenoxybenzyl alpha-bromoisovalerate

Produkt 1

HCID 53935959N-(2-methylphenyl)valine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidLösungsmittel

Versuchsvorschrift

To m-phenoxybenzyl α-bromoisovalerate (2 g, 0.0055 mole), 24°, is added 2-methylaniline (2.95 g, 0.0275 mole) followed by a catalytic amount of potassium iodide (20 mg). The reaction mixture is heated, 110°-115°, for about 36 hours, and then poured into ice-water (30 ml) and 2 N sulfuric acid (10 ml) and extracted with ether (3×30 ml). The combined ether extracts are washed with water (2×30 ml) until neutral and with brine (10 ml) followed by drying over calcium sulfate. The reaction product is concentrated under vacuum and isolated by preparative TLC to yield 3-phenoxybenzyl ester of N-(2-methylphenyl)valine. MS m/e 389.2 (M+).

Aufarbeitung

  1. temperatureThe reaction mixture is heated, 110°-115°, for about 36 hours
  2. extractionextracted with ether (3×30 ml)
  3. washThe combined ether extracts are washed with water (2×30 ml) until neutral and with brine (10 ml)
  4. dry with materialby drying over calcium sulfate
  5. concentrationThe reaction product is concentrated under vacuum
  6. customisolated by preparative TLC

Quellen und Nachweise

ORD-Eintrag
ord-1001254eff5749d68b81cbe7333d1fa5
Quelldatensatz
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04411912

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