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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant9-([2,2'-Binaphthalen]-7-yl)anthraceneHCID 86701353—
CatalystIodineHCID 807—
SolventTetrahydrofuranHCID 8028—
Product9-([2,2'-Binaphthalen]-7-yl)-10-bromoanthraceneHCID 8670135293%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09070885B2
Source datasetuspto-grants-2015_06
ORD IDord-3ff47926326d4d8491c893f22d65442e
Source noteuspto-grants-2015_06