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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383138Generated: October 31, 2026

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

https://huagongshe.com/reaction/1383138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxideHCID 961—
Reactant1,4-DibromobutaneHCID 8056—
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-tetrahydronaphthalen-1-ol (4.2 g, 0.028 mol) in methylene chloride (50 ml) was mixed with a solution of sodum 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 numberUS04808729
Source datasetuspto-grants-1989_02
ORD IDord-98adefce115d43558537414de761415b
Source noteuspto-grants-1989_02