Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | HCID 14602393 | HCID 14602393 | — |
| Reactant | HCID 86746298 | HCID 86746298 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53978061 | HCID 53978061 | — |
Reaction Steps
To a solution of dry pyridine (0.45 mL) in methylene chloride (30 mL) cooled to -15° C. is added trifluoromethanesulfonic anhydride (0.84 mL). The mixture is stirred during 15 min at -10° C., then methyl 2,3,6-tri-O-benzyl-4-deoxy-4-hydroxymethyl-α-D-glucopyranoside (1.19 g, 2.49 mmol) in methylene chloride (5 mL) is added. The mixture is stirred during 1.5 h at -10° C. The reaction mixture is washed with water. The organic layer is dried over sodium sulfate, filtered and concentrated under reduced pressure so as to afford an oil which is the expected triflate methyl 2,3,6-tri-O-benzyl-4-deoxy-4-trifluoromethylsulfonyloxymethyl-α-D-glucopyranoside.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157116 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-527125b14abb4a83a5541f50290b6a9a |
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| Source note | uspto-grants-1992_10 |
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