HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923379Generated: November 2, 2026
N-Fluorobenzenesulfonimide → HCID 118537058, compound
https://huagongshe.com/reaction/923379
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | HCID 86692647 | HCID 86692647 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Oxygen | HCID 977 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118537058 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278980B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f0e64da5c7ec42acb31111251143759e |
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| Source note | uspto-grants-2016_03 |
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