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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047395Generated: November 3, 2026

Water → 1,12-Bis-(12-bromododecyloxy)-dodecane

https://huagongshe.com/reaction/1047395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,12-DibromododecaneHCID 18766—
ReactantSodium hydrideHCID 24758—
Reactant1,12-DodecanediolHCID 79758—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product1,12-Bis-(12-bromododecyloxy)-dodecaneHCID 5949923456%

Reaction Conditions

Temperature80 °C

Reaction Steps

Sodium hydride (60%, 652 mg, 16.3 mmol) washed with hexane was suspended in toluene (3 ml), 1,12-dodecanediol (1.50 g, 7.41 mmol) was added, 1,12-dibromododecane (6.08 g, 18.5 mmol) was added, and the mixture was stirred at 80° C. for 4 days. The reaction mixture was cooled to room temperature, and pure water (30 ml) was added dropwise thereto in a water bath to quench the reaction. The mixture was extracted with chloroform (100 ml), and washed 3 times with 1N hydrochloric acid (30 ml), 3 times with 5% aqueous sodium hydrogen carbonate solution (30 ml), and once with 20% aqueous sodium chloride solution (30 ml). The organic layer was dried over sodium sulfate and the solvent of the filtrate was evaporated. The residue was isolated and purified by silica gel column chromatography, and precipitated with methanol (50 ml) to give 1,12-bis-(12-bromododecyloxy)-dodecane (yield 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569453B2
Source datasetuspto-grants-2013_10
ORD IDord-15bd90b4a2fb43af9daa0763278c968a
Source noteuspto-grants-2013_10