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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858433Generated: October 29, 2026

Sodium Carbonate → 2-{4-[4-(Methylsulfonyl)-2-nitroanilino]phenyl}ethanol

https://huagongshe.com/reaction/858433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Chloro-3-nitrophenyl methyl sulfoneHCID 66796—
Reactant4-Aminophenethyl alcoholHCID 66904—
SolventEthanolHCID 702—
Product2-{4-[4-(Methylsulfonyl)-2-nitroanilino]phenyl}ethanolHCID 2187642834%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-chloro-5-methylsulfonylnitrobenzene (Kavalek, J.; et al. Collect. Czech. Chem. Commun, 1971, 36, 209., 2 g, 8.5 mmol), 4-aminophenylethyl alcohol (1.4 g, 10.2 mmol) and Na2CO3 (1.4 g, 12.7 mmol) in ethanol was stirred at 100° C. for 16 h. The insoluble matter was removed by filtration and washed with ethanol (100 mL). The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel eluting with hexane/ethyl acetate (1:4) to afford 960 mg (34%) of the title compound as yellow solids: 1H-NMR (CDCl3) δ 9.84 (1H, br.s), 8.82 (1H, d, J=2.1 Hz), 7.79 (1H, dd, J=2.1 Hz, 9.1 Hz), 7.36 (2H, d, J=8.4 Hz), 7.22–7.38 (3H, m), 3.94 (2H, br.s), 3.07 (3H, s), 2.93 (2H, t, J=6.6 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148234B2
Source datasetuspto-grants-2006_12
ORD IDord-2a7f1b8cd8b54cd8810f86cfbf9f981d
Source noteuspto-grants-2006_12