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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254130Generated: October 30, 2026

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

https://huagongshe.com/reaction/254130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantSodium HydroxideHCID 14798—
Reactant2-bromo-4H-cyclopenta[def]phenanthreneHCID 12524362—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-bromo-8,9-dihydro-4H-cyclopenta[def]phenanthreneHCID 12524363136.9%

Reaction Steps

2-bromo-4H-cyclopenta[def]phenanthrene (2.6 g, 9.7 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 phase 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, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875367B2
Source datasetuspto-grants-2011_01
ORD IDord-95255682fe1645ac975ab57215ca507a
Source noteuspto-grants-2011_01