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Idramantone → 5-Hydroxy-adamantan-2-one oxime

HRID 12816
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 12816
[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=O)[CH2:3]1)[CH2:9]2.Cl.[NH2:14][OH:15]>CCO.[OH-].[Na+]>[OH:1][C:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C:5]3=[N:14][OH:15])[CH2:3]1)[CH2:9]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 64184IdramantoneHCID 443297Hydroxyamine hydrochloride

Produkt 1

HCID 230089835-Hydroxy-adamantan-2-one oximeAusbeute 73,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 14798Sodium HydroxideLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

5-Hydroxy-2-admantanone (15 g, 90.2 mmol, CAS #: 20098-14-0, purchased from TCI) was dissolved in EtOH (100 mL) and added to a solution of hydroxylamine hydrochloride (10 g, 143.9 mmol) in 1N NaOH (80 mL). The mixture was heated at 100° C. for 2 hours. The EtOH was evaporated, and water and dichloromethane were added. The resulting mixture was stirred for 10 min and then filtered. The solid was collected. The resulting mixture was separated. The aqueous layer was further extracted twice with dichloromethane. The combined organic phases were concentrated under high vacuum. The resulting residue was combined with the solid from the filtration. Crystallization from EtOAc gave 5-hydroxy-adamantan-2-one oxime (12 g, 73%). Mass spectrum: m/z: 182 (M+1).

Aufarbeitung

  1. customThe EtOH was evaporated
  2. additionwater and dichloromethane were added
  3. filtrationfiltered
  4. customThe solid was collected
  5. customThe resulting mixture was separated
  6. extractionThe aqueous layer was further extracted twice with dichloromethane
  7. concentrationThe combined organic phases were concentrated under high vacuum
  8. filtrationThe resulting residue was combined with the solid from the filtration
  9. customCrystallization from EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-c831c44eb924457a978b16137d236615
Quelldatensatz
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07728029B2

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