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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466900Generated: October 30, 2026

Pyridine → HCID 53978061, compound

https://huagongshe.com/reaction/466900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 14602393HCID 14602393—
ReactantHCID 86746298HCID 86746298—
SolventDichloromethaneHCID 6344—
ProductHCID 53978061HCID 53978061—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157116
Source datasetuspto-grants-1992_10
ORD IDord-527125b14abb4a83a5541f50290b6a9a
Source noteuspto-grants-1992_10