ChemicalBook CAS DataBase List 3-BROMO-2-ETHOXYPYRIDINE

3-BROMO-2-ETHOXYPYRIDINE synthesis

6synthesis methods

Product Name:3-BROMO-2-ETHOXYPYRIDINE
CAS Number:57883-25-7
Molecular formula:C7H8BrNO
Molecular Weight:202.05

52200-48-3

64-17-5

141-52-6

57883-25-7

3-Bromo-2-chloropyridine (10.0 g) was used as a raw material, which was dissolved in anhydrous ethanol (100 mL), followed by the slow addition of an ethanol solution of 21% sodium ethoxide (70.8 mL). The reaction mixture was heated to reflux and kept reacting overnight. After completion of the reaction, the solvent was removed by rotary evaporator under reduced pressure. The residue was dissolved in ethyl acetate and washed sequentially with saturated aqueous sodium bicarbonate and aqueous ammonium chloride. The organic layer was dried with anhydrous sodium sulfate, filtered and the solvent evaporated to give the crude product. The crude product was purified by silica gel column chromatography with the eluent of cyclohexane/ethyl acetate (10:1, v/v) to give 3-bromo-2-ethoxypyridine (7.26 g, 69% yield) as a yellow oil. The product was characterized by 1H-NMR (400 MHz, DMSO-d6): δ[ppm] = 1.34 (t, 3H), 4.37 (q, 2H), 6.93 (dd, 1H), 8.02 (dd, 1H), 8.15 (dd, 1H).

13534-89-9
326 suppliers
$6.00/1g

64-17-5 Synthesis

64-17-5
856 suppliers
$10.00/50g

57883-25-7
114 suppliers
$72.50/250mg

Yield:57883-25-7 85%

Reaction Conditions:

with sodium for 12 h;Reflux;

Steps:

3-Bromo-2-ethoxypyridine (4a); Typical Procedure

General procedure: Na (2.40 g, 105 mmol) was slowly dissolved in anhyd EtOH (100 mL)while stirring. Then, 2,3-dibromopyridine (7.11 g, 30.0 mmol) wasadded and the reaction mixture was refluxed for 12 h. After quenchingwith sat. aq NH4Cl, the product was extracted with EtOAc. Thecombined organic extracts were dried (Na2SO4) and evaporated invacuo. The crude product obtained was purified by flash chromatography(n-pentane:EtOAc 9:1) to give 4a as a yellow liquid; yield: 5.15g (25.5 mmol, 85%).IR (Diamond-ATR, neat): 2978, 1581, 1471, 1444, 1429, 1381, 13511314, 1297, 1251, 1243, 1068, 1035, 1019, 928, 781, 750, 690 cm-1.1H NMR (400 MHz, CDCl3): = 8.07 (dd, J = 4.9, 1.7 Hz, 1 H), 7.79 (dd,J = 7.6, 1.7 Hz, 1 H), 6.74 (dd, J = 7.6, 4.9 Hz, 1 H), 4.43 (q, J = 7.0 Hz, 2H), 1.43 (t, J = 7.1 Hz, 3 H).13C NMR (101?MHz, CDCl 3): = 159.9, 145.6, 141.7, 117.6, 107.3, 63.0,14.7.MS (EI, 70 eV): m/z (%) = 188 (98), 186 (100), 175 (34), 153 (35), 159(19), 157 (19), 147 (57), 145 (59), 78 (37).HRMS (EI): m/z [M - CH3]+ calcd for C6H5BrNO: 185.9555; found:185.9548

References:

Heinz, Benjamin;Djukanovic, Dimitrije;Siemens, Fiona;Idriess, Mohamed;Martin, Benjamin;Knochel, Paul [Synthesis,2021,vol. 54,# 22,p. 5055 - 5063]

36178-05-9 Synthesis