2-Bromo-4-methoxypyridine synthesis
- Product Name:2-Bromo-4-methoxypyridine
- CAS Number:89488-29-9
- Molecular formula:C6H6BrNO
- Molecular Weight:188.02
620-08-6
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Yield: 62%
Reaction Conditions:
Stage #1:4-methoxypyridine with n-butyllithium;2-(N,N-dimethylamino)ethanol in hexane at -20; for 1 h;Inert atmosphere;
Stage #2: with 1,2-dibromo-1,1,2,2-tetrachloroethane in tetrahydrofuran;hexane at -78 - 20;Inert atmosphere;
Steps:
4-Methoxy-2-bromopyridine (2).
A solution of N,N-dimethylethanolamine (1.40 mL, 13.93 mmol) in hexanes (10 mL) at -20 oC was treated with n-BuLi (11.91 mL, 27.86 mmol, 2.34M in hexanes). The reaction mixture was stirred under nitrogen for 30 minutes. Neat 4-methoxypyridine (0.70 mL, 6.90 mmol) was added dropwise. The orange solution was stirred for one hour and then cooled to -78 oC. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (5.40 g, 16.57 mmol) in THF (5 mL) was added dropwise, and the mixture was allowed to slowly warm to room temperature overnight. The reaction was quenched with water at 0 oC and extracted with diethyl ether. The combined extracts were dried over anhydrous magnesium sulfate and concentrated. The desired product was distilled (70 °C, 3 mmHg) to yield 0.81 g (62%) of 2 as yellow oil. 1H NMR (300 MHz, CDCl3) δ 3.86 (s, 3H), 6.78-6.80 (dd, J 2.1, 2.4, 5.9 Hz, 1H), 7.00-7.01 (d, J 2.4 Hz, 1H), 8.16-8.18 (d, J 6.0 Hz, 1H);13C NMR (75 MHz, CDCl3) δ 55.6, 110.2, 113.2, 143.0, 150.6, 166.8; FTIR (film) 2321, 2350, 2371, 2851, 2925,2956 cm-1; HRMS (FAB) calcd for C6H6BrNO (M+1) 187.9711; found 187.9708.
References:
Bori, Ibrahim D.;Comins, Daniel L. [Arkivoc,2021,vol. 2021,p. 57 - 72]
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