Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Magnesium diiodide | HCID 5462737 | — |
| Reactant | HCID 86745554 | HCID 86745554 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86745555 | HCID 86745555 | — |
Reaction Steps
To a solution of methyl 2,3,4-tri-O-benzyl-6-deoxy-7-O-methylsulfonyl-α-D-glucoheptopyranoside (0.38 g, 0.83 mmol) in ether (5 ml) was added at 0° C. a 0.375 M solution of magnesium iodide (6.7 ml). The mixture was stirred 15 min at 0° C. The excess of magnesium iodide was hydrolyzed with water. The reaction mixture was washed with sodium thiosulfate and Water. The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure to afford an oil. Flash chromatography on silica gel and elution with a 2:8 mixture of ethyl acetate and hexane afforded the expected iodide methyl 2,3,4-tri-O-benzyl-6,7-dideoxy-7-iodo-α-D-glucoheptopyranoside which was crystallized from hexane (0.368 g, 91%); m.p. 66°-68° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05504078 |
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| Source dataset | uspto-grants-1996_04 |
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| ORD ID | ord-8c3b5a4675264a2fb3a1f226dc52d7a9 |
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| Source note | uspto-grants-1996_04 |
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