zinc(II) iodide in benzene Rearrangement; 1 h; Heating;

<b>With</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '608317', constants.ctx, '0')">3-chloro-benzenecarboperoxoic acid</a>&nbsp;<b>in</b>&nbsp; <a href="#" onclick="return RXDsubstances(event, this, '1730800', constants.ctx, '0')">dichloromethane</a> <br />Epoxidation;&nbsp;1.5&nbsp;h;&nbsp;<br /> &nbsp;

<b>Multi-step reaction with 2 steps<br /> </b>1: p-toluenesulfonic acid (p-TSA) / toluene / 1 h / Heating<br />2: 96 percent / m-chloroperbenzoic acid (m-CPBA) / CH₂Cl₂ / 1.5 h<br /> <br /> &nbsp;

<b>Multi-step reaction with 3 steps<br /> </b>2: p-toluenesulfonic acid (p-TSA) / toluene / 1 h / Heating<br />3: 96 percent / m-chloroperbenzoic acid (m-CPBA) / CH₂Cl₂ / 1.5 h<br /> <br /> &nbsp;

<b>Multi-step reaction with 3 steps<br /> </b>2: p-toluenesulfonic acid (p-TSA) / toluene / 1 h / Heating<br />3: 96 percent / m-chloroperbenzoic acid (m-CPBA) / CH₂Cl₂ / 1.5 h<br /> <br /> &nbsp;