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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650192Generated: October 31, 2026

Hexane → 4-(1-Naphthoyl)-3,5-dichlorotoluene

https://huagongshe.com/reaction/1650192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant3,5-DichlorotolueneHCID 32834—
Reactant1-Naphthalenecarbonyl chlorideHCID 70146—
SolventTetrahydrofuranHCID 8028—
SolventButyllithiumHCID 178418339—
Product4-(1-Naphthoyl)-3,5-dichlorotolueneHCID 14700029104.1%

Reaction Conditions

Temperature-60 °C

Reaction Steps

To a stirred, cold (-60° C.) solution of 3,5-dichlorotoluene (3.5 g, 21.7 mmol) in dry tetrahydrofuran (30 ml), 2.6 M n-butyllithium in hexane (8.78 ml, 22.8 mmol) was added dropwise over 15 minutes. The reaction mixture was stirred for one hour at -60° C. and then treated with a solution of 1-naphthoyl chloride (4.14 g, 21.7 mmol) in 15 ml of dry tetrahydrofuran over a period of 15 minutes. The mixture was stirred for 3.5 hours at -60° C. and then quenched with 4.8 ml of saturated NH4Cl solution. The mixture was permitted to warm to room temperature and then diluted with 30 ml of water and 30 ml of ether. The layers were thoroughly mixed and then separated. The etheral layer was backed-washed with brine and dried with anhydrous magnesium sulfate. Concentration afforded 7.12 g of crude product which was chromatographed on silica gel (20:1 hexane:ethyl acetate) to give 1.59 g (23 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04923885
Source datasetuspto-grants-1990_05
ORD IDord-f97f253af5084068965eced3708b300f
Source noteuspto-grants-1990_05