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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865859Generated: October 25, 2026

1-Bromohexane → 2-Bromo-6-(hexyloxy)naphthalene

https://huagongshe.com/reaction/865859

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-2-naphthalenolHCID 27144—
SolventDimethylformamideHCID 6228—
Product2-Bromo-6-(hexyloxy)naphthaleneHCID 453558381%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 4.46 g (20.0 mmol) of 6-bromo-2-naphthalenol (obtained from Aldrich Chemical Company (#B7,340-6) and used without purification), in 20 mL of DMF at room temperature under argon was added 480 mg (20 mmol) of 95% sodium hydride over the course of 15 min. The resulting light yellow solution was stirred 30 min and 3.5 mL (22 mmol) of 1-bromohexane was added. The reaction was heated to 50° C. and stirred for 60 min. The reaction was quenched with ice water, the resultings solids filtered, washed with water and dried in vacuo at 60° C. Purification of the residue by chromatography on silica gel (5×20 cm column, hexanes as elutant) gave 5.00 g, 81% yield, of title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05567841
Source datasetuspto-grants-1996_10
ORD IDord-366c43619d6748c8a70aa5bba187dba9
Source noteuspto-grants-1996_10