HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179855Generated: October 31, 2026
Sodium Thiosulfate → 9-([2,2'-Binaphthalen]-7-yl)-10-bromoanthracene
https://huagongshe.com/reaction/2179855
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 9-([2,2'-Binaphthalen]-7-yl)anthracene | HCID 86701353 | — |
| Catalyst | Iodine | HCID 807 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 9-([2,2'-Binaphthalen]-7-yl)-10-bromoanthracene | HCID 86701352 | 93% |
Reaction Steps
Under the nitrogen atmosphere, 9-([2,2′-binaphthalen]-7-yl) anthracene (10.0 g) as the ninth intermediate compound, N-bromosuccinimide (NBS) (4.6 g), iodine (0.1 g), and THF (60 ml) were added to a flask and stirred overnight at room temperature. By adding an aqueous solution of sodium thiosulfate, the reaction was terminated. Liquid separation was performed by adding water and toluene. Subsequently, the solid obtained by distillation of the organic layer under reduced pressure was purified by silica gel column chromatography (solvent: toluene). The solid obtained by distillation of the solvent under reduced pressure was washed with heptane to give 9-([2,2′-binaphthalen]-7-yl)-10-bromoanthracene (11.0 g) as a tenth intermediate compound. The scheme is shown in the following “Reaction 15”.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09070885B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-3ff47926326d4d8491c893f22d65442e |
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| Source note | uspto-grants-2015_06 |
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