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ChemicalBook CAS DataBase List 6-Methoxy-2-vinylnaphthalene
63444-51-9

6-Methoxy-2-vinylnaphthalene synthesis

12synthesis methods
-

Yield: 84%

Reaction Conditions:

with (1,2-dimethoxyethane)dichloronickel(II);18-crown-6 ether;potassium methanolate in N,N-dimethyl-formamide at 35; for 12 h;Inert atmosphere;Hiyama Coupling;Reagent/catalyst;Solvent;

Steps:

General Procedure 1
General procedure: In a nitrogen-filled glove box, aromatic halide (0.2 mmol, 1.0equiv), 18-crown-6 (121.0 mg, 0.46 mmol, 2.3 equiv), KOMe(32.2 mg, 0.46 mmol, 2.3 equiv), NiCl2(glyme) (4.4 mg, 0.02mmol, 10 mol%), and DMF (1.0 mL) were charged to an 8 mL vialequipped with a magnetic stirrer bar. The vinyltrimethoxysilane(68.0 mg, 0.46 mmol, 2.3 equiv) was added. The vial wasremoved from the glove box, and the reaction mixture wasstirred at rt (35 °C) for 12 h. The reaction mixture was thendiluted with EtOAc and washed with water. The organic phasewas dried over Na2SO4, filtered, and concentrated, and theresidue was purified by column chromatography on silica gel togive the product.2-Methoxy-6-vinylnaphthalene (3a)Using general procedure 1: white solid, 31.0 mg, yield: 84%. 1HNMR (400 MHz, CDCl3): = 7.78-7.66 (m, 3 H), 7.62 (dd, J = 8.7,1.7 Hz, 1 H), 7.19-7.10 (m, 2 H), 6.87 (dd, J = 17.6, 10.9 Hz, 1 H),5.84 (dd, J = 17.6, 0.9 Hz, 1 H), 5.30 (dd, J = 10.9, 0.9 Hz, 1 H),3.93 (s, 3 H).

References:

Wei, Shichao;Mao, Yongjun;Shi, Shi-Liang [Synlett,2021,art. no. ST-2020-K0612-C] Location in patent:supporting information

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