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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223478Generated: October 26, 2026

Mannitol → Mannitol monocarbonate

https://huagongshe.com/reaction/2223478

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 numberUS07375133B2
Source datasetuspto-grants-2008_05
ORD IDord-11cd7d05f7504de9892d27ca3e678ab7
Source noteuspto-grants-2008_05