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Mannitol → Mannitol monocarbonate

HRID 857587
Notes
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Reaction equation

HRID 857587 reaction equation
CC1C(=[O:8])[C@@H](O)CC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/C1C(C)(C)C[C@H](O)C(=O)C=1C.CCN(C(C)C)C(C)C.Cl[C:55]([O:57]C(Cl)C(Cl)(Cl)Cl)=[O:56].[CH2:64]([OH:75])[C@H:65]([C@H:67]([C@@H:69]([C@@H:71]([CH2:73][OH:74])[OH:72])[OH:70])[OH:68])[OH:66]>C(Cl)Cl.CN(C1C=CN=CC=1)C.CN(C=O)C>[C:55](=[O:56])([OH:8])[OH:57].[CH2:73]([OH:74])[C@H:71]([C@H:69]([C@@H:67]([C@@H:65]([CH2:64][OH:75])[OH:66])[OH:68])[OH:70])[OH:72]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 4

HCID 6251MannitolHCID 81531DiisopropylethylamineHCID 27333271,2,2,2-Tetrachloroethyl chloroformateHCID 5281224Astaxanthin

Product 1

HCID 86594020Mannitol monocarbonateYield 10.19%

Reagents, catalysts & solvents 3

HCID 14284
4-(Dimethylamino)pyridine
Catalyst
HCID 6228DimethylformamideSolvent
HCID 6344DichloromethaneSolvent2×

Conditions

Temperature
0 °C

Procedure

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%).

Workup

  1. waitat room temperature for 1.5 hours
  2. stirringThe reaction mixture was stirred at room temperature for 24 hours, at which time the reaction
  3. customquenched with brine (20 mL)
  4. extractionextracted with DCM
  5. concentrationThe combined organic layers were concentrated

Sources & evidence

ORD record
ord-1d0f8210da6d4ad386a59e203537d222
Source dataset
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07145025B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes