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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25660Erstellt: 23. Oktober 2026

Acetic Acid → 5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acid

https://huagongshe.com/de/reaction/25660

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium hydrideHCID 24758—
Edukt(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
Edukttert-butyl N-methyl-N-(4-oxocyclohexyl)carbamateHCID 24820328—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acidHCID 2256768285,6%

Reaktionsschritte

5 g (21.99 mmol) Methyl-(4-oxo-cyclohexyl)-carbamic acid tert-butyl ester and 12.68 g (28.59 mmol) (4-Carboxy-butyl)-triphenyl-phosphonium bromide were dispended in 50 ml DMF. In small portions 2.49 g (57.2 mmol, 55%) NaH were added and the slurry was diluted by adding 50 ml DMF. The mixture was stirred at RT over night, 10 ml AcOH were added and the solvent was evaporated under reduced pressure. The residue was dissolved in ether and water, and the inorganic layer was extracted with ether. The combined organic phases were dried over and the crude materil was purified by column chromatography with ETOAc/hexane to give 5.86 g (83%)5-[4-(tert-Butoxycarbonyl-methyl-amino)-cyclohexylidene]-pentanoic acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858651B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-6ed6edff7c4840dc8c5284f235649c74
Quellennotizuspto-grants-2005_02