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2-Bromo-4-isopropoxy-1-methylbenzene synthesis

2synthesis methods
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Yield:1254062-68-4 98%

Steps:



3-Bromo-4-methylphenol was reacted with isopropyl iodide to afford 98% of 2- bromo-4-isopropoxy-l-methylbenzene. 1H-NMR (400 MHz, CDCl3) δ (ppm): 7.106- 7.085 (m, 2H), 6.751-6.726 (dd, IH, J=IO, 1.6 Hz), 4.483-4.452 (m, IH), 2.312 (s, 3H), 1.317-1.302 (d, 6H, J=6 Hz).

References:

WO2010/127212,2010,A1 Location in patent:Page/Page column 41