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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379349Generated: November 1, 2026

3-Nitrobenzoic acid → 1-(1,1-Dimethylethylsulphonylaminocarbonyl)-3-nitrobenzene

https://huagongshe.com/reaction/2379349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrobenzoic acidHCID 8497—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactanttert-ButylsulfonamideHCID 2757335—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(1,1-Dimethylethylsulphonylaminocarbonyl)-3-nitrobenzeneHCID 1895778085%

Reaction Steps

To a mixture of 3-nitrobenzoic acid (0.37 g, 2.2 mmol), 1,1-dimethylethylsulphonamide (0.3 g, 2.2 mmol) and 4-dimethylaminopyridine (0.27 g, 2.2 mmol) in anhydrous dichloromethane (20 ml), under an atmosphere of nitrogen, was added. 1-[3-(dimethylamino)propyl]-3-ethyl carbodiimide hydrochloride (0.42 g, 2.2 mmol). The mixture was stirred at ambient temperature for 22 h. The mixture was extracted with 1M NaOH (50 ml) and the separated aqueous phase acidified using 5M HCl. This was extracted with dichloromethane (5×20 ml), then the combined organic extracts were dried (Na2SO4) and evaporated to dryness. The residue was chromatographed on silica gel using 1% methanol in dichloromethane as the eluant. The title compound (0.53 g, 85%) was isolated as a colourless solid. mp 220° C. 1H NMR (360 MHz, D6-DMSO) δ 1.27 (9H, s), 6.59 (1H, brs), 7.65 (1H, t, J=7.9 Hz), 8.24-8.30 (1H, m), 8.34-8.38 (1H, m), 8.68-8.72 (1H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05360802
Source datasetuspto-grants-1994_11
ORD IDord-6418b30647d4438193b56c2333ae2ed4
Source noteuspto-grants-1994_11