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ChemicalBook CAS DataBase List 3-Bromo-4-chloropyridine
36953-42-1

3-Bromo-4-chloropyridine synthesis

8synthesis methods
31270-80-1 Synthesis
4-CHLOROFURO[3,2-C]PYRIDINE

31270-80-1
116 suppliers
$10.00/100mg

220939-72-0 Synthesis
3-Bromo-4-chlorofuro[3,2-c]pyridine

220939-72-0
39 suppliers
$62.00/250mg

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Yield:36953-42-1 96%

Reaction Conditions:

with sodium hydroxide;bromine in methanol;tetrachloromethane

Steps:

543.A 3-bromo-4-chlorofuro[3,2-c]pyridine
EXAMPLE 543A 3-bromo-4-chlorofuro[3,2-c]pyridine A solution of 4-chlorofuro[3,2-c]pyridine (commercially available, 10.60 g, 69 mmol) in carbon tetrachloride (135 mL) was cooled to -15° C. and bromine (12.13 g, 80 mmol) was added drop-wise over a fifteen minute time period. The mixture was stirred at ambient temperature for eighteen hours. The solvent was removed in vacuo, and the residue was dissolved in methanol (250 mL). A solution of 20% aqueous sodium hydroxide (35 mL) was added and the mixture was stirred 1 hour at ambient temperature. The methanol was removed in vacuo, and the residue was partitioned between water (100 mL) and dichloromethane (50 mL). The combined organic layers were dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to give 3-bromo-4-chloro[3,2-c]pyridine 15.45 g, 96%) as a solid. MS (ESI(+)) m/e 232, 234 (M+H)+.

References:

Betschmann, Patrick;Burchat, Andrew F.;Calderwood, David J.;Curtin, Michael L.;Davidsen, Steven K.;Davis, Heather M.;Frey, Robin R.;Heyman, Howard R.;Hirst, Gavin C.;Hrnciar, Peter;Michaelides, Michael R.;Muckey, Melanie A.;Rafferty, Paul;Wada, Carol K. US2005/26944, 2005, A1

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