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Sodium Hydroxide → 4-Boc-2-methyl-1-phenylpiperazine

HRID 2416656
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2416656
[CH3:1][CH:2]1[N:7]([C:8]2[CH:13]=[CH:12][C:11](N)=[CH:10][CH:9]=2)[CH2:6][CH2:5][N:4]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:3]1.N([O-])=O.[Na+].[OH-].[Na+]>[PH2](O)=O.O.[Cu-]=O>[CH3:1][CH:2]1[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:6][CH2:5][N:4]([C:15]([O:17][C:18]([CH3:19])([CH3:21])[CH3:20])=[O:16])[CH2:3]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 14798Sodium HydroxideHCID 22633057(+/-)-tert-Butyl 3-methyl-4-(4-aminophenyl)piperazine-1-carboxylateHCID 23668193Sodium Nitrite

Produkt 1

HCID 226330714-Boc-2-methyl-1-phenylpiperazine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178419072HCID 178419072, VerbindungKatalysator
HCID 962
Water
Lösungsmittel
HCID 4124402Phosphinic AcidLösungsmittel

Versuchsvorschrift

To a solution of (±)-tert-butyl 3-methyl-4-(4-aminophenyl)piperazine-1-carboxylate (325 mg) in 50% hypophosphorous acid (1.27 ml) containing copper(I) oxide (8.0 mg) was added dropwise a solution of sodium nitrite (92 mg) in water (2 ml) at 0° C. with stirring. After 2 hours, the reaction mixture was made alkaline with 40% NaOH solution and extracted with ethyl acetate twice. The organic layers were combined and washed with water and brine. The solvent was evaporated, and the residue was purified by silica gel column chromatography (hexane-ethyl acetate 1:1) to give the title compound in a pure form as colorless oil.

Aufarbeitung

  1. extractionextracted with ethyl acetate twice
  2. washwashed with water and brine
  3. customThe solvent was evaporated
  4. customthe residue was purified by silica gel column chromatography (hexane-ethyl acetate 1:1)

Quellen und Nachweise

ORD-Eintrag
ord-af3dad8bbe5a48e8995131070a264a16
Quelldatensatz
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06825200B1

Notizen zur Reaktion

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