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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923379Generated: November 2, 2026

N-Fluorobenzenesulfonimide → HCID 118537058, compound

https://huagongshe.com/reaction/923379

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-FluorobenzenesulfonimideHCID 588007—
ReactantHCID 86692647HCID 86692647—
ReactantButyllithiumHCID 178418339—
SolventOxygenHCID 977—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118537058HCID 118537058—

Reaction Steps

In an alternate embodiment, a method is described of producing a monomer wherein the method begins by dissolving 3-fluoro-4,6 dihydrothieno[3,4-b]thiophene in tetrahydrofuran in a non-oxygen atmosphere to create a solution. An initiator of n-butyllithium is then added to the solution to produce an initiated solution. This is followed by adding N-fluorobenzenesulfonimide to the initiated solution to produce 2,3-difluoro-4,6-dihydrothieno[3,4-b]thiophene. 2,3-difluoro-4,6-dihydrothieno[3,4-b]thiophene is then oxidized with meta-chloroperoxybenzoic acid to produce 2,3-difluorothieno[3,4-b]thiophene. 2,3-difluorothieno[3,4-b]thiophene is then bromoated with N-bromosuccinimide to produce 4,6-dibromo-2,3-difluorothieno[2,3-c]thiophene. The final step involves debrominating 4,6-dibromo-2,3-difluorothieno[2,3-c]thiophene and adding an aryl group to produce the monomer

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278980B2
Source datasetuspto-grants-2016_03
ORD IDord-f0e64da5c7ec42acb31111251143759e
Source noteuspto-grants-2016_03