Synlett 2014; 25(17): 2503-2507
DOI: 10.1055/s-0034-1379205
letter
© Georg Thieme Verlag Stuttgart · New York

Generation of Aryl Grignard Reagents from Arene Chromium Tricarbonyl Complexes by Mg(TMP)2·2LiCl and Their Application to Murahashi Coupling

Yuichi Momoi
Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki, Aoba-ku, 980-8578 Sendai, Japan   Fax: +81(22)7956877   Email: tokuyama@mail.pharm.tohoku.ac.jp
,
Kentaro Okano
Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki, Aoba-ku, 980-8578 Sendai, Japan   Fax: +81(22)7956877   Email: tokuyama@mail.pharm.tohoku.ac.jp
,
Hidetoshi Tokuyama*
Graduate School of Pharmaceutical Sciences, Tohoku University, Aramaki, Aoba-ku, 980-8578 Sendai, Japan   Fax: +81(22)7956877   Email: tokuyama@mail.pharm.tohoku.ac.jp
› Author Affiliations
Further Information

Publication History

Received: 18 August 2014

Accepted: 04 September 2014

Publication Date:
18 September 2014 (online)


Abstract

A mild and straightforward synthesis of biaryls is described that is performed through direct arylation of the C–H bond of (arene)Cr(CO)3 upon deprotonation with Mg(2,2,6,6-tetramethylpiperazide)2·2LiCl and subsequent palladium-catalyzed cross-coupling reaction.

 
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  • 22 Synthesis of (Biaryl)Cr(CO)3 9a: A 30 mL two-necked round-bottomed flask equipped with a magnetic stirring bar was charged with 7a (249 mg, 1.02 mmol) and THF (1.0 mL). To the solution was added freshly prepared Mg(TMP)2·2LiCl (0.10 M in THF, 11 mL, 1.1 mmol) dropwise over 5 min at 0 °C. The resulting mixture was stirred at 0 °C for 1 h. To the yellow solution was added CuI (114 mg, 0.60 mmol) portionwise at 0 °C. After the mixture was stirred at 0 °C for 1 h, methyl p-iodobenzoate (13a; 524 mg, 2.0 mmol) and Pd(PPh3)4 (117.9 mg, 102 μmol) were added and the reaction mixture was stirred at r.t. for 1 h. The reaction was quenched with sat. aq NH4Cl, and the mixture was stirred for 10 min. The resulting mixture was filtered through a Celite pad and the filtrate was extracted with Et2O. The combined organic extracts were washed with brine, dried over anhydrous Na2SO4, and filtered. The filtrate was concentrated under reduced pressure to give a crude black solid, which was purified by silica gel column chromatography (EtOAc–hexanes, 1:3 to 1:1) to provide (biaryl)Cr(CO)3 9a (353 mg, 0.915 mmol, 90%) as a dark-red solid. IR (neat): 1955, 1862 (CO stretch), 1715, 1279, 1251, 1111, 825, 773, 662 cm–1; 1H NMR (400 MHz, CDCl3): δ = 8.04 (d, J = 8.0 Hz, 2 H), 7.60 (d, J = 8.0 Hz, 2 H), 5.75 (d, J = 6.8 Hz, 1 H), 5.63 (dd, J = 6.8, 6.8 Hz, 1 H), 5.13 (d, J = 6.8 Hz, 1 H), 4.98 (dd, J = 6.8, 6.8 Hz, 1 H), 3.93 (s, 3 H), 3.76 (s, 3 H); 13C NMR (100 MHz, CDCl3): δ = 232.3, 166.3, 141.1, 138.8, 130.1, 129.7, 129.0, 99.7, 97.7, 94.2, 84.2, 72.9, 55.7, 51.9; MS (EI): m/z = 378 [M]+; HRMS (EI): m/z [M]+ calcd for C18H14CrO6: 378.0196; found: 378.0184.