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Potassium Iodide → N-(2,6-dimethylphenyl)valine

HRID 648246
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 648246
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]=[C:27]([CH3:31])[C:25]=1[NH2:26].[I-].[K+]>S(=O)(=O)(O)O>[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[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 68962,6-DimethylanilineHCID 13229492m-Phenoxybenzyl alpha-bromoisovalerate

Produkt 1

HCID 15383894N-(2,6-dimethylphenyl)valine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1118Sulfuric AcidLösungsmittel

Versuchsvorschrift

To m-phenoxybenzyl α-bromoisovalerate (2 g, 0.0055 mole), 24°, is added 2,6-dimethylaniline (3.33 g, 0.0275 mole) followed by a catalytic amount of potassium iodide (20 mg). The reaction mixture is heated at about 120° for 48 hours, and then poured into ice-water (20 ml) and 2 N sulfuric acid (10 ml) and extracted with ether (3×30 ml). The combined ether extracts are washed with water (2×20 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 give m-phenoxybenzyl ester of N-(2,6-dimethylphenyl)valine. MS m/e 403.2 (M+, 7.5).

Aufarbeitung

  1. temperatureThe reaction mixture is heated at about 120° for 48 hours
  2. extractionextracted with ether (3×30 ml)
  3. washThe combined ether extracts are washed with water (2×20 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-c8307741d2bc43d89e84e8c13752c8d1
Quelldatensatz
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04411912

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