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Acetic Acid → (R)-1-(4-bromo-benzoyl)-2-methyl-azetidine-2-carboxylic acid

HRID 408582
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 408582
C[O:2][C:3]([C@@:5]1([CH3:9])[CH2:8][CH2:7][NH:6]1)=[O:4].[OH-].[Na+].[Br:12][C:13]1[CH:21]=[CH:20][C:16]([C:17](Cl)=[O:18])=[CH:15][CH:14]=1.C(O)(=O)C>O>[Br:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]([N:6]2[CH2:7][CH2:8][C@:5]2([CH3:9])[C:3]([OH:2])=[O:4])=[O:18])=[CH:15][CH:14]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 685154-Bromobenzoyl chlorideHCID 70556683methyl (2R)-2-methylazetidine-2-carboxylate

Produkt 1

HCID 70557656(R)-1-(4-bromo-benzoyl)-2-methyl-azetidine-2-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

To a solution of (R)-2-methyl-azetidine-2-carboxylic acid methyl ester (1 eq.) in water were added aqueous NaOH (1M) (3 eq.) then 4-bromo-benzoyl-chloride (1 eq.) dropwise. The reaction was stirred for 4 h at 20° C. The reaction was neutralised with acetic acid. The solvent was partially removed under reduced pressure and the crude was extracted with EtOAc. The organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with DCM/MeOH/AcOEt/AcOH/iPr2O: 95/5/98/2/300) to afford (R)-1-(4-bromo-benzoyl)-2-methyl-azetidine-2-carboxylic acid.

Aufarbeitung

  1. customThe solvent was partially removed under reduced pressure
  2. extractionthe crude was extracted with EtOAc
  3. dry with materialThe organic layer was dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe crude was purified by chromatography on silica gel (elution with DCM/MeOH/AcOEt/AcOH/iPr2O: 95/5/98/2/300)

Quellen und Nachweise

ORD-Eintrag
ord-94275a0954b04b7baad270064a8b1dde
Quelldatensatz
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08759334B2

Notizen zur Reaktion

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