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Sodium Hydroxide → HCID 178453623, Verbindung

HRID 271360
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 271360
[C:1]([O:5][C:6]([NH:8][CH2:9][C@@H:10]1[CH2:15][CH2:14][C@H:13]([C:16]([O:18]CCCC)=[O:17])[CH2:12][CH2:11]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>CO>[C:1]([O:5][C:6]([NH:8][CH2:9][C@@H:10]1[CH2:11][CH2:12][C@H:13]([C:16]([OH:18])=[O:17])[CH2:14][CH2:15]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 178451157HCID 178451157, Verbindung

Produkt 1

HCID 178453623HCID 178453623, VerbindungAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of crude butyl cis-4-{[(tert-butoxycarbonyl)amino]methyl}cyclohexanecarboxylate (28.4 g, approximately 79.3 mmol) in methanol (200 ml) was added dropwise over five minutes 2N sodium hydroxide solution (400 mmol). The mixture was stirred 18 hours at ambient temperature under nitrogen. The mixture was concentrated under reduced pressure to remove methanol. To the aqueous residue was added methyl orange (1 mg) and 3N hydrochloric acid was added to adjust the mixture to pH 4. The mixture was extracted with ethyl acetate (3×200 ml). The extract was washed with water (100 ml), and brine (100 ml), dried (sodium sulfate), filtered, and the solvent evaporated under reduced pressure to give cis-4-{[(tert-butoxycarbonyl)amino]methyl}cyclohexanecarboxylic acid (18.76 g, 92%) as an off-white solid. MS: 258.3 (M+1).

Aufarbeitung

  1. concentrationThe mixture was concentrated under reduced pressure
  2. customto remove methanol
  3. additionTo the aqueous residue was added methyl orange (1 mg) and 3N hydrochloric acid
  4. additionwas added
  5. extractionThe mixture was extracted with ethyl acetate (3×200 ml)
  6. washThe extract was washed with water (100 ml), and brine (100 ml)
  7. dry with materialdried (sodium sulfate)
  8. filtrationfiltered
  9. customthe solvent evaporated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-021e51cbf7c3496aac3d8fd3f88ad31f
Quelldatensatz
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07452893B2

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