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ChemicalBook CAS DataBase List 2-methoxy-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
755030-94-5

2-methoxy-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile synthesis

3synthesis methods
-

Yield:755030-94-5 65%

Reaction Conditions:

with potassium acetate;(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride in dimethyl sulfoxide at 80; for 2 h;

Steps:

267.267C Example 267; 2-[3-(4-cyano-3-methoxyphenyl)-11-oxo-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-8-yl]-2-methyl-N-(4-morpholin-4-ylphenyl)propanamide; Example 267C; 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

Example 267B (2. 0g, 7.7 mmol), bis (pinacolato) -diboron, (2.2g, 8.7 mmol), KOAC (2.2g, 22.4 mmol), and PDCL2 (DPPF)-CH2CI2 (315 mg, 0.39 mmol) in DMSO (40 mL) was heated at 80 C for 2 hours. The reaction was then cooled, filtered through CELITE then partitioned between toluene and water. The organic layer was washed with brine, dried over NA2SO4, filtered and concentrated to give 2.3g crude material. That crude was stirred in 50 C hexane (35 mL) for 1 hour, filtered, and the filtrate was allowed to cool to room temperature, then placed in the refigerator overnight. Recovered 1.3g (65%) grayish-brown crystals. MS (DCI) M/E 277 (M+NH4) + ; 1H NMR (300 MHz, DMSO-D6) 8 7.73 (d, J=7.8 Hz, 1H), 7.35 (m, 2H), 3.93 (s, 3H), 1.32 (s, 12H).

References:

WO2004/76424,2004,A1 Location in patent:Page 181

6609-56-9 Synthesis
2-Methoxybenzonitrile

6609-56-9
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2-methoxy-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

755030-94-5
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1220219-22-6 Synthesis
3-Cyano-4-methoxyphenylboronic acid pinacol ester

1220219-22-6
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