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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1671747Erstellt: 26. Oktober 2026

Chloroform → N-lauroyl-L-valine cyclohexylamide

https://huagongshe.com/reaction/1671747

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktCyclohexylamineHCID 7965—
EduktN-(1-Oxododecyl)-L-valineHCID 26658—
EduktN-Hydroxysuccinimide hydrateHCID 18987794—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-lauroyl-L-valine cyclohexylamideHCID 1152376444%

Reaktionsschritte

61 mg (0.20 mmol) of N-lauroyl-L-valine and 39 mg (0.26 mmol) of N-hydroxysuccinimide monohydrate were dissolved into 3.0 mL of dried chloroform. 50 mg (0.26 mmol) of 1-ethyl-3-(3-dimethylpropyl)carbodiimide hydrochloride was added thereto under argon atmosphere and in the ice bath, and stirred at 0° C. for 3 hours. 35 μL of triethylamine and 35 μL of cyclohexylamine were added thereto and stirred at room temperature overnight. Then, 20 mL of ethyl acetate was added thereto and washed with 25 mL of 0.2N hydrochloric acid, 20 mL of water and 20 mL of a saturated aqueous solution of sodium hydrogen carbonate. The mixture was then dried with anhydrous sodium sulfate and condensed under reduced pressure. The residue was purified with a thin-layer chromatography (silica gel, chloroform:methanol=20:1) to obtain 34 mg of N-lauroyl-L-valine cyclohexylamide (0.089 mmol, yield 44%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07994353B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-9354f11cead54404a1a6b46abc7bb267
Quellennotizuspto-grants-2011_08