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Hydroxyamine hydrochloride → HCID 178453351, Verbindung

HRID 632417
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 632417
C(=O)(O)[O-].[Na+].Cl.[NH2:7][OH:8].[C:9]([O:13][C:14](=[O:24])[NH:15][C:16]([C:22]#[N:23])([CH2:18][CH:19]1[CH2:21][CH2:20]1)[CH3:17])([CH3:12])([CH3:11])[CH3:10]>CCO.O>[C:9]([O:13][C:14](=[O:24])[NH:15][C:16]([C:22](=[NH:23])[NH:7][OH:8])([CH3:17])[CH2:18][CH:19]1[CH2:20][CH2:21]1)([CH3:10])([CH3:12])[CH3:11]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 71087668(Cyano-cyclopropylmethyl-methyl-methyl)-carbamic acid tert-butyl ester

Produkt 1

HCID 178453351HCID 178453351, VerbindungAusbeute 65,5 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittel2×
HCID 962
Water
Lösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Sodium bi carbonate (0.204 g, 2.9 mmol) was dissolved in EtOH (10 mL) and water (10 mL). Hydroxylamine hydrochloride (0.204 g, 2.9 mmol) was added at 25° C. A solution of (cyano-cyclopropylmethyl-methyl-methyl)-carbamic acid tert-butyl ester (3) (0.7 g, 2.67 mmol) in ethanol (5 mL) was added thereto and the resulting reaction mixture was heated at 80° C. for 12 hours. After evaporation of solvents, the residue was dissolved in ethyl acetate (30 mL) and then filtered. The filtrate was concentrated in vacuo. The residue was purified by chromatography (Combi-Flash, 40 g, 5:95 ethyl acetate/n-hexane) to give the title compound (0.45 g, 65%) as white solid; LC-MS (ELSD peak area, ESI) 100%, 258.2 [M+H]+.

Aufarbeitung

  1. customthe resulting reaction mixture
  2. customAfter evaporation of solvents
  3. dissolutionthe residue was dissolved in ethyl acetate (30 mL)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo
  6. customThe residue was purified by chromatography (Combi-Flash, 40 g, 5:95 ethyl acetate/n-hexane)

Quellen und Nachweise

ORD-Eintrag
ord-7e79c4cea3a444d58af3df3fd175d0fa
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09321727B2

Notizen zur Reaktion

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