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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650235Generated: November 1, 2026

1,4-Dibromobutane → 5-(4-Bromobutoxy)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/1650235

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium HydroxideHCID 14798—
Reactant5,6,7,8-Tetrahydro-1-naphtholHCID 68258—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-(4-Bromobutoxy)-1,2,3,4-tetrahydronaphthaleneHCID 14405945102.1%

Reaction Steps

A solution of 5,6,7,8 tetrahydronaphthalene-1-ol (4.2 g, 0.028 mol) in methylene chloride (50 ml) was mixed with a solution of sodium hydroxide (2.3 g, 0.0575 mol) in water (50 ml). After adding tetra-n butylammonium bisulfate (9.6 g, 0.028 mol) and 1,4-dibromobutane (31 g, 0.14 mol), the reaction mixture was refluxed with vigorous stirring for 2 hrs. The reaction was cooled to room temperature, the layers separated and the organic phase washed with saturated sodium chloride solution. After drying over sodium sulfate, the organic phase was concentrated on the rotary evaporator and the residual oil heated under vacuum (0.1 mm Hg) to remove remaining 1,4-dibromobutane. The residue was chromatographed on silica gel using 100% hexane as eluent to give 8.1 g (71%) of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923891
Source datasetuspto-grants-1990_05
ORD IDord-ee9f81b569284cba8416cf1ee581f2f6
Source noteuspto-grants-1990_05