Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate → Ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate

HRID 21979

Reaktionsgleichung

Reaktionsgleichung von HRID 21979
[C:1]([O:5][C:6]([CH:8]=[C:9]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH:12]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[NH:11][C:10]1=[O:24])=[O:7])([CH3:4])([CH3:3])[CH3:2]>C(OCC)(=O)C.[Pd]>[C:1]([O:5][C:6]([CH2:8][CH:9]1[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH:12]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[NH:11][C:10]1=[O:24])=[O:7])([CH3:3])([CH3:4])[CH3:2]

Komponenten

4

Versuchsvorschrift

Ethyl 3-t-butoxycarbonylmethylidene-2-oxo-1-azacyclodecane-10-carboxylate (2.85 g, 8.4 mmol) is dissolved in ethyl acetate (75 mL). 10% Pd/C (2.0 g) is added, and the reaction is stirred under an atmosphere of hydrogen for 4.5 hours. The reaction is filtered through Celite, and the solvent is removed. The crude product is purified by silica gel chromatography (20% ethyl acetate/hexane) to give separately the two diastereomers of ethyl 3-t-butoxycarbonylmethyl-2-oxo-1-azacyclodecane-10-carboxylate.

Aufarbeitung

  1. filtrationThe reaction is filtered through Celite
  2. customthe solvent is removed
  3. customThe crude product is purified by silica gel chromatography (20% ethyl acetate/hexane)

Quellen und Nachweise

ORD-Eintrag
ord-816f91b6ed0f4caeb76cd0aee3ce2eb8
Quelldatensatz
uspto-grants-1995_06
Patentnummer
US05426103

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