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59255-98-0

2-tert-butyl-4-nitrobenzenamine synthesis

6synthesis methods
N-(2-tert-butyl-4-nitrophenyl)acetamide

815586-43-7
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2-tert-butyl-4-nitrobenzenamine

59255-98-0
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Yield:59255-98-0 100%

Reaction Conditions:

with hydrogen bromide in water at 110; for 3 h;

Steps:

3.3

N-(2-tert-butyl-4-nitrophenyl)acetamide (840 mg, 3.57 mmol) was dissolved in concentrated HBr (48%, 20 mL). The resulting solution was heated at 110° C. for 3 h. The reaction mixture was cooled to rt, diluted with EtOAc, and poured into sat. NaHCO3 solution. The organic phase was extracted with sat. NaHCO3 solution and brine, dried over Na2SO4, filtered and concentrated to give the desired product as a yellow-green oil (710 mg, >100%). 1H NMR (400 MHz, CD3OD) δ: 7.52 (d, 1H), 7.40 (dd, 1H), 7.33 (d, 1H), and 1.42 (s, 9H).

References:

US2006/160803,2006,A1 Location in patent:Page/Page column 137

253185-04-5 Synthesis
Benzene, (1,1-dimethylethyl-13C)- (9CI)

253185-04-5
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2-tert-butyl-4-nitrobenzenamine

59255-98-0
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