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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670165Generated: October 27, 2026

1-Bromooctane → 2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene

https://huagongshe.com/reaction/1670165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantSodium HydroxideHCID 14798—
Reactant2,6-dibromo-4H-cyclopenta[def]phenanthreneHCID 59431076—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthreneHCID 12524367133.6%

Reaction Steps

2,6-dibromo-4H-cyclopenta[def]phenanthrene (2.6 g, 7.7 mmol) and octyl bromide (3.6 g, 18.5 mmol) in a 50 ml round bottom flask were dissolved with toluene (10 ml), and TBAB (tetrabutylammoniumbromide) (0.125 g, 0.385 mmol) was added thereto. A solution of NaOH (3.1 g, 77 mmol) in water (50 ml) was added to the reaction mixture, and the resultant solution was refluxed for two days. After the reaction was terminated, the reaction solution was extracted with chloroform. The organic layer was dried over MgSO4, concentrated, and purified by silica gel column chromatography (eluent: n-hexane). The eluate was distilled under a reduced pressure to remove unreacted octyl bromide, thereby giving a compound 2 (3.6 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07990053B2
Source datasetuspto-grants-2011_08
ORD IDord-f4854494cbe54643b7756f8390d6d00d
Source noteuspto-grants-2011_08