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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2186661Erstellt: 26. Oktober 2026

1,2-Dichloroethane → (1S,2S)-2-(7-oxooctanoyl)amino-3-morpholino-1-phenyl-1-propanol

https://huagongshe.com/reaction/2186661

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktTriethylamineHCID 8471—
Edukt7-Oxooctanoic acidHCID 26464—
Edukt(1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanolHCID 10513992—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1S,2S)-2-(7-oxooctanoyl)amino-3-morpholino-1-phenyl-1-propanolHCID 6982132459,1%

Reaktionsschritte

A mixed solvent of methylene chloride:methanol=9:1 (20 ml), 7-oxooctanoic acid (700 mg, 4.4 mmol), triethylamine (1.40 ml, 10.0 mmol) and EDC (1.15 g, 6.0 mmol) were added to (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol (944.0 mg, 4.0 mmol), followed by stirring overnight. Methylene chloride (100 ml) was added to the reaction solution. After washed with a saturated sodium hydrogen carbonate solution (50 ml), water (50 ml) and saturated brine (50 ml) successively, the organic layer was dried over sodium sulfate and filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform:ethanol=20:1) to obtain the title compound (890 mg, yield 59%) as colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06407064B2
Quelldatensatzuspto-grants-2002_06
ORD IDord-46f28482c5de43128f1566b914bbe8e9
Quellennotizuspto-grants-2002_06