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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 735220Erstellt: 24. Oktober 2026

Mannitol → Mannitol monocarbonate

https://huagongshe.com/de/reaction/735220

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMannitolHCID 6251—
EduktDiisopropylethylamineHCID 81531—
Edukt1,2,2,2-Tetrachloroethyl chloroformateHCID 2733327—
EduktAstaxanthinHCID 5281224—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktMannitol monocarbonateHCID 8659402010,19%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of astaxanthin 2E (0.100 g, 0.168 mmol) in DCM (4 mL) at 0° C. was added DIPEA (0.585 mL, 3.36 mmol), and 1,2,2,2-tetrachloroethyl chloroformate (0.103 mL, 0.672 mmol). The reaction mixture was stirred at 0° C. for 2 hours, then at room temperature for 1.5 hours, at which time (D)-mannitol (0.3060 g, 1.68 mmol), DMF (3 mL), and DMAP (0.2052 g, 1.68 mmol) were added to the reaction. The reaction mixture was stirred at room temperature for 24 hours, at which time the reaction was diluted with DCM, quenched with brine (20 mL), and then extracted with DCM. The combined organic layers were concentrated to yield mannitol monocarbonate (LVII) (10.19%) HPLC retention time: 9.474 min., 10.19% (AUC); LRMS (ESI) m/z (relative intensity): 827 (M++Na) (50), 804 (M+) (25), 725 (58), 613 (100), and astaxanthin (53.73%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07592449B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-a32bfa06c6ea47a3afd9db4fcef6b0b9
Quellennotizuspto-grants-2009_09