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2-AMino-6-broMo-2-(2-chlorophenyl)cyclohexanone-d4 HydrobroMide synthesis

4synthesis methods
6740-86-9 Synthesis
1-bromocyclopentyl-o-chlorophenyl ketone

6740-86-9
60 suppliers
$377.00/5g

2-AMino-6-broMo-2-(2-chlorophenyl)cyclohexanone-d4 HydrobroMide

79499-60-8
8 suppliers
inquiry

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Yield:-

Steps:

Multi-step reaction with 3 steps
1: 1) liq. NH3, 2) HCl / 1) 4 h, 2) i-PrOH
2: 88 percent / various solvent(s) / 0.12 h / 180 °C
3: 82 percent / 48percent aq. HBr, Br2 / 0.17 h / 70 °C

References:

Parcell, Robert F.;Sanchez, Joseph P. [Journal of Organic Chemistry,1981,vol. 46,# 25,p. 5055 - 5060]