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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 413402Erstellt: 25. Oktober 2026

N-(tert-butoxycarbonyl)glycine → N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl ester

https://huagongshe.com/reaction/413402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(tert-butoxycarbonyl)glycineHCID 78288—
Eduktcis-4-Benzyloxy-2-buten-1-olHCID 11008492—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl esterHCID 69891095—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

N-[(1,1-Dimethylethoxy)carbonyl]glycine (21.9 grams, 0.125 mol), cis-4-benzyloxy-2-buten-1-ol (25 mL, 0.15 mol), and 4-dimethylaminopyridine (1.5 grams, 0.013 mol) are dissolved in methylene chloride and stirred at 0° C. Then N,N-dicyclohexylcarbodiimide (31 grams, 0.15 mol) in 30 mL methylene chloride is added and the reaction is stirred at 0° C. for five minutes. The reaction is then stirred for an additional twelve hours at 25° C. Additional methylene chloride is added and the reaction is washed consecutively with 1 N HCl, sodium bicarbonate and then with brine. The organic extract is dried over magnesium sulfate and the solvent evaporated in vacuo to give an orange oil which is absorbed onto silica gel and applied to a dry silica column. The column is eluted with hexane/EtOAc (9:1) then with hexane/EtOAc (8:2) Product fractions are combined and dried in vacuo to give the desired product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06566381B1
Quelldatensatzuspto-grants-2003_05
ORD IDord-fc51b361b1384d3aa246311f51cb3677
Quellennotizuspto-grants-2003_05