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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098371Generated: November 2, 2026

1,6-Dibromohexane → 1-(4-((6-Bromohexyl)oxy)butyl)-4-nitrobenzene

https://huagongshe.com/reaction/2098371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium HydroxideHCID 14798—
ReactantSulfate, hydrogenHCID 61778—
Reactant4-NitrobenzenebutanolHCID 590869—
SolventDichloromethaneHCID 6344—
Product1-(4-((6-Bromohexyl)oxy)butyl)-4-nitrobenzeneHCID 2007142420.1%

Reaction Steps

A stirred mixture of 4-(4-nitrophenyl)butan-1-ol (2.0 g, 10 mmol), tetra-n-butylammomium hydrogen sulfate (0.17 g, 0.5 mmol), and 1,6-dibromohexane (3.2 mL, 20 mmol) in dichloromethane (10 mL) was treated with aqueous sodium hydroxide solution (10 M, 1 mL). The reaction mixture was stirred for 6 days at room temperature. The organic and aqueous phases were separated. The aqueous phase was extracted thrice with dichloromethane. The combined organics were washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The crude residue was purified via automated flash silica gel chromatography, using a 40 g SiliSep flash column (hexanes/ethyl acetate). Concentration of the desired fractions under reduced pressure provided the title compound as a pale straw-colored oil (0.72 g, 20%). ES/MS calcd. for C16H25BrNO3+ 358.1, found m/z=358.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450490B2
Source datasetuspto-grants-2013_05
ORD IDord-6574d84d57ee48a69752935ea8c12987
Source noteuspto-grants-2013_05