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Sodium Hydroxide → HCID 17952314, Verbindung

HRID 1371525
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1371525
C[O:2][C:3](=[O:17])[CH2:4][CH:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][N:6]1[CH:14]([CH3:16])[CH3:15].[OH-].[Na+]>CO>[CH:14]([N:6]1[CH2:7][C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:5]1[CH2:4][C:3]([OH:17])=[O:2])([CH3:16])[CH3:15]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 69219063(2-isopropyl-2,3-dihydro-1H-isoindol-1-yl)-acetic acid methyl ester

Produkt 1

HCID 17952314HCID 17952314, VerbindungAusbeute 85,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To the compound of Step B (0.53 g., 2.30 mmol) in MeOH (5.1 mL) was added 1.0N NaOH (2.53 mL, 2.53 mmol). After two days, the solution was concentrated to dryness. The resulting residue was diluted with 1.0N HCl and water was loaded onto a strong cation exchange resin. The resin was washed with water, THF/water (1:1) and then water. The product was then eluted from the resin with pyridine/water (1:9). The eluent was concentrated to dryness to afford about 0.43 g (85%) of the final compound. EIS-MS 220 [M+1].

Aufarbeitung

  1. concentrationthe solution was concentrated to dryness
  2. additionThe resulting residue was diluted with 1.0N HCl and water
  3. washThe resin was washed with water, THF/water (1:1)
  4. washThe product was then eluted from the resin with pyridine/water (1:9)
  5. concentrationThe eluent was concentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-8bcb1402882249828d79357509759ef8
Quelldatensatz
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07157463B2

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