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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762662Generated: October 27, 2026

1-Methoxynaphthalene → 2-(4-Chlorobutyl)-1-methoxynaphthalene

https://huagongshe.com/reaction/1762662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethoxynaphthaleneHCID 16668—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-4-chlorobutaneHCID 81364—
ReactantButyllithiumHCID 178418339—
SolventCyclohexaneHCID 8078—
Product2-(4-Chlorobutyl)-1-methoxynaphthaleneHCID 1561793739%

Reaction Steps

A solution of N,N,N',N'-tetramethylenediamine (18.12 mL, 0.120 mole) in cyclohexane (36 mL) was treated with n-butyllithium (1.55M in hexane; 79.8 mL, 0.123 mole) at room temperature. A solution of 1-methoxynaphthalene (17.4 mL, 0.120 mole) in cyclohexane (20 mL) was added over 30 minutes, and the resulting solution was stirred for 1.5 hours. It was then cooled to 0°, and 1-bromo-4-chlorobutane (27.0 mL, 0.234 mole) was added over 15 minutes. The mixture was warmed to room temperature and stirred for 17 hours, then poured into saturated aqueous ammonium chloride and extracted with ethyl acetate. The crude product was chromatographed with 98:2 hexane/ether to provide the title compound (11.60 g, 39%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04833164
Source datasetuspto-grants-1989_05
ORD IDord-b101681c0ff548128676520f8d555784
Source noteuspto-grants-1989_05