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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179862Generated: November 1, 2026

Sodium Thiosulfate → 2-(10-Bromoanthracen-9-yl)triphenylene

https://huagongshe.com/reaction/2179862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-bromobutanimideHCID 67184—
Reactant2-(Anthracen-9-yl)triphenyleneHCID 86701357—
CatalystIodineHCID 807—
SolventTetrahydrofuranHCID 8028—
Product2-(10-Bromoanthracen-9-yl)triphenyleneHCID 8670135888.8%

Reaction Steps

Under the nitrogen atmosphere, 2-(anthracen-9-yl)triphenylene (3.3 g) as the eleventh intermediate compound, N-bromosuccinimide (NBS) (1.7 g), iodine (0.1 g) and THF (25 ml) were added to a flask, and stirred at room temperature for 5 hours. An aqueous solution of sodium thiosulfate was added and the reaction was terminated. The precipitates were collected by suction filtration. The obtained solid was washed with methanol and subsequently with heptane and purified by silica gel column chromatography (solvent: toluene) to give 2-(10-bromoanthracen-9-yl)triphenylene (3.5 g) as a twelfth intermediate compound. The scheme is shown in the following “Reaction 22”.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09070885B2
Source datasetuspto-grants-2015_06
ORD IDord-be85ceab0e8c4df4bde8abdf2f5fa34d
Source noteuspto-grants-2015_06