4-Nitroaniline → N-(4-nitrophenyl)methanesulfonamide

4-Nitro-phenylamine (25 g, 181 mmol) was dissolved in pyridine (450 mL). Methanesulfonyl chloride (14.0 mL, 181 mmol) was added dropwise while stirring. The mixture was stirred for 16 h at 25° C. The solution was concentrated in vacuo to a volume of ˜50 mL. The mixture was diluted with ethyl acetate (400 mL), washed with 1.0 M aqueous hydrochloric acid solution (5×200 mL). The combined aqueous layers were back-extracted with ethyl acetate (200 mL). The combined organic layers were dried over magnesium sulfate, filtered and concentrated in vacuo to a volume of ˜250 mL. The product precipitated and was collected by vacuum filtration. The filtrate was concentrated in vacuo to a volume of ˜125 mL upon which additional product precipitated. The solid was collected by vacuum filtration. The solids were combined to afford the desired product, N-(4-nitro-phenyl)-methanesulfonamide (25 g, 115.62 mmol, 64% yield) as a pale yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 3.17 (3H, s), 7.35 (2H, d, J=9.4 Hz), 8.20 (2H, d, J=9.1 Hz), 10.69 (1H, s).

1. stirringThe mixture was stirred for 16 h at 25° C
2. concentrationThe solution was concentrated in vacuo to a volume of ˜50 mL
3. additionThe mixture was diluted with ethyl acetate (400 mL)
4. washwashed with 1.0 M aqueous hydrochloric acid solution (5×200 mL)
5. extractionThe combined aqueous layers were back-extracted with ethyl acetate (200 mL)
6. dry with materialThe combined organic layers were dried over magnesium sulfate
7. filtrationfiltered
8. concentrationconcentrated in vacuo to a volume of ˜250 mL
9. customThe product precipitated
10. filtrationwas collected by vacuum filtration
11. concentrationThe filtrate was concentrated in vacuo to a volume of ˜125 mL upon which additional product
12. customprecipitated
13. filtrationThe solid was collected by vacuum filtration

ORD record

ord-3aa535289cdd4e9fa559212d8edf1a21

Source dataset

uspto-grants-2009_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07582754B2