Benzenamine, 3-bromo-4-methyl- → 5-Bromo-2-iodo-4-methylaniline

A solution of 3-bromo-4-methylaniline (5.00 g, 26.9 mmol), N-iodosuccinimide (4.53 g, 20.2 mmol) and bis(pyridine)iodonium tetrafluoroborate (2.70 g, 7.26 mmol) in DCM (100 mL) was stirred at room temperature overnight. The mixture was diluted with DCM, washed sequentially with saturated aqueous NaHSO3 and water, and dried and concentrated. The residue was purified by column chromatography on silica gel, eluting with EtOAc-hexanes (sequentially 1%, 2% and 3%), to provide 5-bromo-2-iodo-4-methylaniline as a yellow solid (5.27 g, 63% yield). Mass spectrum m/z 312, 314 (M+H)+. 1H NMR (500 MHz, CDCl3) δ 7.49 (d, J=0.6 Hz, 1H), 6.94 (s, 1H), 4.17-3.91 (br.s, 2H), and 2.25 (s, 3H).

1. washwashed sequentially with saturated aqueous NaHSO3 and water
2. customdried
3. concentrationconcentrated
4. customThe residue was purified by column chromatography on silica gel
5. washeluting with EtOAc-hexanes (sequentially 1%, 2% and 3%),

ORDレコード

ord-6b1c575cf99143dd801aea8b8ea68062

出典データセット

uspto-grants-2016_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09334290B2