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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381061Generated: November 3, 2026

Toluene → 2-Heptyl-6-(5-ethyl-2-pyrimidinyl)naphthalene

https://huagongshe.com/reaction/1381061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 23323276HCID 23323276—
SolventMethanolHCID 887—
Product2-Heptyl-6-(5-ethyl-2-pyrimidinyl)naphthaleneHCID 1353132560%

Reaction Conditions

Temperature60 °C

Reaction Steps

NaOH (1.1 g, 26 mmols) was added to anhydrous methanol (40 ml) and dissolved therein by heating to 60° C. with stirring. To the solution was added 6-heptyl-2-naphthalenecarboxamidine hydrochloride (4.0 g, 13 mmols) to prepare a suspension with stirring. To this suspension was dropwise added over one minute a solution obtained by dissolving α-ethyl-β-dimethylaminoacrolein (1.7 g, 13 mmols) in anhydrous methanol (5 ml), followed by gently refluxing the mixture with stirring for 2 hours, distilling off methanol under the atmospheric pressure after completion of the reaction, adding toluene (50 ml) to the residue to extract the resulting product, washing the extraction solution with a 2N-NaOH aqueous solution and then with water, drying over anhydrous sodium sulfate, and distilling off toluene under reduced pressure to obtain solids, which were then recrystallized from ethanol to obtain the objective 2-heptyl-6-(5-ethyl-2-pyrimidinyl)naphthalene (2.5 g, 7.8 mmols) (yield: 60%). M.P.: 62.3°-63.1° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585575
Source datasetuspto-grants-1986_04
ORD IDord-d593f3f4dc2447a4b3d428c7e9c53007
Source noteuspto-grants-1986_04