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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 129068Erstellt: 26. Oktober 2026

Salicylamide → o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide

https://huagongshe.com/reaction/129068

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicylamideHCID 5147—
EduktTriphenylphosphineHCID 11776—
EduktDi-tert-butyl azodicarboxylateHCID 97268—
Edukt3-Hexyl-4-((R)-2-hydroxytridecyl)-2-oxetanone, (3S,4S)-HCID 10428248—
LösungsmittelTetrahydrofuranHCID 8028—
Produkto-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamideHCID 5413350449,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

1.1 g of (3S,4S)-3-hexyl-4-[(R)-2-hydroxytridecyl]-2-oxetanone, 1.6 g of triphenylphosphine, 0.825 g of salicylamide and 3 g of molecular sieve (4 Å) were treated with 20 ml of THF and cooled to 0° C. Thereupon, 1.4 g of di-t-butyl azodicarboxylate were added. After warming to room temperature and stirring the reaction mixture was concentrated and the residue was partitioned between methanol/water (70:30) and hexane and extracted with hexane. The hexane phase was dried and concentrated and the residue was chromatographed on silica gel with hexane/ethyl acetate (4:1). There were obtained 0.727 g of o-[[(S)-1-[[(2S,3S)-3-hexyl-4-oxo-2-oxetanyl]methyl]dodecyl]oxy]-benzamide, MS: 474 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05466708
Quelldatensatzuspto-grants-1995_11
ORD IDord-5ec19bf755b94c5ca8e7a8d5d56850b2
Quellennotizuspto-grants-1995_11