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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250879Generated: October 25, 2026

Mannitol → Mannitol monocarbonate

https://huagongshe.com/reaction/2250879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMannitolHCID 6251—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,2,2,2-Tetrachloroethyl chloroformateHCID 2733327—
ReactantAstaxanthinHCID 5281224—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductMannitol monocarbonateHCID 8659402010.19%

Reaction Conditions

Temperature0 °C

Reaction Steps

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 2E (53.73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317008B2
Source datasetuspto-grants-2008_01
ORD IDord-deb742026a6d4337a68c34d3e141487a
Source noteuspto-grants-2008_01