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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Nitrobenzoic acid | HCID 8497 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | tert-Butylsulfonamide | HCID 2757335 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1,1-Dimethylethylsulphonylaminocarbonyl)-3-nitrobenzene | HCID 18957780 | 85% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05360802 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-6418b30647d4438193b56c2333ae2ed4 |
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| Source note | uspto-grants-1994_11 |
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