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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1476362Generated: October 31, 2026

Tetrahydrofuran → 2-Decyl-6-methoxynaphthalene

https://huagongshe.com/reaction/1476362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-BromodecaneHCID 8173—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantHCID 178418384HCID 178418384—
CatalystHCID 178418745HCID 178418745—
SolventWaterHCID 962—
Product2-Decyl-6-methoxynaphthaleneHCID 86704381—

Reaction Steps

A THF solution of n-decyl magnesium bromide (prepared as a THF (2 ml) solution of n-decyl bromide (2.2 ml, 11 mmol) and Mg (292 mg, 12 mmol)) was added to 6-bromo-2-methoxynaphthalene (2.37 g, 10 mmol) easily available from a reagent manufacturer and a THF (10 ml) solution of Ni(dppp)Cl2 (271 mg, 0.5 mmol), and the mixture was heated under reflux for 19 hours. After cooling, the mixed solution was diluted with water (10 ml), and non-reacted Mg was filtered out. The filtered solution was extracted with ether (5 ml×3). The extracted organic phases were collected (10 ml×3), and dried with MgSO4, and condensed with an evaporator. The condensed organic phase was recrystallized with hexane to obtain 6-n-decyl-2-methoxynaphthalene (compound (3)-64) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018630B2
Source datasetuspto-grants-2015_04
ORD IDord-0a539def97724f5f858adcdbbc2c0a6c
Source noteuspto-grants-2015_04