Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Mannitol | HCID 6251 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,2,2,2-Tetrachloroethyl chloroformate | HCID 2733327 | — |
| Reactant | Astaxanthin | HCID 5281224 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Mannitol monocarbonate | HCID 86594020 | 10.19% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07145025B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-1d0f8210da6d4ad386a59e203537d222 |
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| Source note | uspto-grants-2006_12 |
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