N-bromobutanimide → 2-Chloro-4-bromo-5-methyl-6-fluoroaniline

2-Chloro-5-methyl-6-fluoroaniline (23 g, 0.14 mol) and N-bromosuccinimide (25 g, 0.14 mol) are dissolved with stirring in 200 mL of anhydrous DMF. The reaction mixture is stirred overnight and then most of the DMF is removed by rotary evaporator under high vacuum. The dark brown residue is partitioned between 1:1 Et2O/hexane (500 mL) and water (500 mL). The organic layer is washed with brine (5×250 mL), dried (MgSO4) and concentrated by rotary evaporator. The crude material is purified using flash chromatography (20% CH2Cl2/hexanes) and then further purified by bulb-to-bulb distillation (b.p. 155–165° C. at ˜20 mm of Hg) to give 2-chloro-4-bromo-5-methyl-6-fluoroaniline as a peach-colored solid which is re-crystallized from ice-cold hexanes (m.p. 67–71° C.).

1. custommost of the DMF is removed by rotary evaporator under high vacuum
2. customThe dark brown residue is partitioned between 1:1 Et2O/hexane (500 mL) and water (500 mL)
3. washThe organic layer is washed with brine (5×250 mL)
4. dry with materialdried (MgSO4)
5. concentrationconcentrated by rotary evaporator
6. customThe crude material is purified
7. distillationfurther purified by bulb-to-bulb distillation (b.p. 155–165° C. at ˜20 mm of Hg)

ORD record

ord-302c5f3a536e4bd89f5e27a633bf2c31

Source dataset

uspto-grants-2007_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07202364B2