Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 644788Erstellt: 25. Oktober 2026

Triphenylphosphine → 4-(6-Morpholin-4-ylhexyl)-salicylamide

https://huagongshe.com/reaction/644788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktSodium HydroxideHCID 14798—
Edukt2H-1,3-Benzoxazine-2,4(3H)-dioneHCID 16258—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt4-MorpholinehexanolHCID 22218504—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(6-Morpholin-4-ylhexyl)-salicylamideHCID 6707040137,2%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A slurry of carsalam (6.13 g, 37.6 mmol), 4-(6-hydroxyhexyl)morpholine (7.0 g, 37.4 mmol), triphenylphosphine (9.97 g, 35.0 mmol), and tetrahydrofuran (40 mL) was treated with a solution of diisopropyl azodicarboxylate (7.40 mL, 7.60 g, 37.6 mmol) and tetrahydrofuran (10 mL), added dropwise over 15 minutes. The reaction mixture was stirred at 25° C. for 60 hours. The solution was treated with aqueous 2N NaOH (50 mL, 100 mmol) and warmed to 60° C. for 180 minutes. The cooled reaction mixture was concentrated to remove the tetrahydrofuran. The aqueous residue was washed with ethyl acetate (2×40 mL), and was acidified with 4% aqueous HCl to a pH of 0.84 (causing carbon dioxide gas to evolve). The pH of the aqueous phase was raised to 7.8 with 2N aqueous NaOH. Solid sodium bicarbonate was added. Extraction with ethyl acetate (8×40 mL), drying over sodium sulfate and concentration gave an oil which solidified upon standing. A total of 4.26 g of 4-(6-morpholin-4-ylhexyl)-salicylamide was isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07700775B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-4410d9785cd14ba78083bb38ac16f57d
Quellennotizuspto-grants-2010_04