Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525982Generated: October 30, 2026

Dichloromethane → 9,10-Bis(octyloxy)anthracene

https://huagongshe.com/reaction/525982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant1-IodooctaneHCID 12380—
ReactantSodium HydroxideHCID 14798—
ReactantSodium DithioniteHCID 24489—
CatalystTrioctylmethylammonium chlorideHCID 21218—
Product9,10-Bis(octyloxy)anthraceneHCID 2130420125%

Reaction Steps

To nitrogen saturated water (100 ml) and dichloromethane (100 ml) 9,10-anthraquinone (2.02 g, 9.61 mmol), sodium dithionite (3.39 g, 19.5 mmol), and Adogen 464 (3.5 g) was added. This was stirred for 5 minutes before addition of sodium hydroxide (3.8 g, 95.0 mmol). The reaction mixture was stirred for an additional 10 min and when it turned deep red 1-iodooctane (11.5 g, 47.9 mmol) was added drop wise. The reaction was stirred at room temperature under nitrogen atmosphere over night. The phases were separated and the water phase was extracted two times with dichloromethane and then the combined organic phases were washed two times with water and evaporated to obtain oil with crystals. These were recrystallised in ethanol and removed as starting material. After two crops the ethanol solution was cooled and the ensuing yellow crystals was purified by column chromatography using dichloromethane as mobile phase to yield 9,10-dioctyloxyanthracene (1.3 g, 2.99 mmol) as a white solid. 1H NMR (CDCl3, δ): 0.91 (t, 6H), 1.2-1.45 (m, 16H), 1.64 (m, 4H), 2.04 (m, 4H), 4.16 (t, 4H), 7.46 (m, 4H), 8.28 (m, 4H) MS MALDI-TOF (m/z): 434.247

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09343198B2
Source datasetuspto-grants-2016_05
ORD IDord-87810cd4ff494cd2a4ea8f01a0437519
Source noteuspto-grants-2016_05