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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039302Generated: November 1, 2026

Trifluoromethanesulfonic anhydride → HCID 59611359, compound

https://huagongshe.com/reaction/2039302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 59611582HCID 59611582—
SolventPyridineHCID 1049—
ProductHCID 59611359HCID 59611359—

Reaction Steps

Tf2O was added slowly to a mixture of 2-(4-bromo-phenyl)-benzo[b]thiophen-6-ol (200 mg, 0.66 mol) in pyridine (3 mL) at 0° C. with stirring. The mixture was stirred at ambient temperature for 16 hours before quenched with NaHCO3 solution. The mixture was extracted with ethyl acetate (50 mL). The organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. The obtained residue was used for next step reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575118B2
Source datasetuspto-grants-2013_11
ORD IDord-e2db83d3e9fc4a2b8c8b48b65ceab5b4
Source noteuspto-grants-2013_11