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METHYL 2-BROMO-1-ETHYL-1H-IMIDAZOLE-5-CARBOXYLATE synthesis

2synthesis methods
METHYL 2-BROMO-1-ETHYL-1H-IMIDAZOLE-5-CARBOXYLATE

1398414-98-6
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Yield:-

Reaction Conditions:

with N-Bromosuccinimide;2,2'-azobis(isobutyronitrile) in tetrachloromethane at 50; for 4 h;

Steps:

33

The preceeding ester (265 mg, 1.7 mmol) NBS (612 mg, 3.4 mmol), and AIBN (15 mg, 0.1 mmol) are combined in CC14 (30 mL), and then heated to 50 °C for 4 h. The reaction is filtered hot through a short pad of diatomaceous earth, rinsing with additional CC14, then concentrated in vacuo to afford crude bromide 33-115 (450 mg).

References:

WO2012/122340,2012,A1 Location in patent:Page/Page column 87