Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 980116Erstellt: 25. Oktober 2026

Triethylamine → 3-(4-Propyl-heptyl)-4-(5-hydroxypentyl)morpholine

https://huagongshe.com/reaction/980116

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTriethylamine hydrochlorideHCID 11130—
Edukt3-(4-Propylheptyl)morpholineHCID 11096343—
EduktGlutaric acid monomethylester chlorideHCID 53445129—
LösungsmittelBenzeneHCID 241—
LösungsmittelDiethyl EtherHCID 3283—
Produkt3-(4-Propyl-heptyl)-4-(5-hydroxypentyl)morpholineHCID 14721997—

Reaktionsschritte

A mixture of 8.0 grams (0.035 moles) of 3-(4-propyl-heptyl)-morpholine, 4 grams of triethylamine, 5.8 grams (0.035 moles) of glutaric acid-monomethylesterchloride and 100 ml. of benzene were refluxed for 3 hours. After cooling the triethylamine hydrochloride formed was removed by filtration and the benzene solution was directly admixed with 12 grams of lithium aluminum hydride in 500 ml of ether. The reaction mixture was refluxed for 8 hours and decomposed by slow addition of water and sodium hydroxide. The precipitate was filtered off. The ether solution was dried and evaporated to dryness and the residue was distilled at 144°-146° C./0.01 mm Hg.; yield 9.8 grams (89%). The base obtained was dissolved in ether and the hydrochloride precipitated with hydrochloric acid in ethanol. After recrystallization from ethylacetate/ether, the melting point was 59°-60° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04636382
Quelldatensatzuspto-grants-1987_01
ORD IDord-fde9f904850e4b8b81baafc56b79659b
Quellennotizuspto-grants-1987_01