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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 968524Erstellt: 25. Oktober 2026

1-Phenyl-1-propanol → (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid phenylpropyl ester

https://huagongshe.com/reaction/968524

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Phenyl-1-propanolHCID 7147—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acidHCID 69415969—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid phenylpropyl esterHCID 6941712164,4%

Reaktionsschritte

0.301 g (1 mmol) of (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid, 0.204 g (1.5 mmol) of phenylpropanol, 0.088 g (0.33 mmol) of CAS, 0.227 g (1.2 mmol) of DCC and 0.04 g (0.33 mmol) of DMAP were dissolved in 15 mL of CH2Cl2. The mixture was stirred for 24 h at room temperature. The solid was filtrated and the solvent was evaporated. The residual was dissolved in a suitable amount of ethyl acetate (20 ml) and then the mixture was filtered to remove insoluble substance. The ethyl acetate was added to 60 ml and then the liquid was washed with 10% NaHCO3 solution, saturated NaCl solution and dried over Na2SO4. After the drying agent was removed and part of ethyl acetate was evaporated, the crude product was purified by flash column chromatography (eluent: ethyl acetate:cyclohexane=2:1) to obtain the product as a oil (0.27 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07304057B2
Quelldatensatzuspto-grants-2007_12
ORD IDord-8747625e82b74c538fa91990af8999e0
Quellennotizuspto-grants-2007_12