HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1985767Erstellt: 26. Oktober 2026
Citric Acid → N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide
https://huagongshe.com/reaction/1985767
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Citric Acid | HCID 311 | — |
| Edukt | Nitric Acid | HCID 944 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Edukt | Cyclopropylamine | HCID 69828 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Produkt | N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide | HCID 8469273 | 92% |
Reaktionsschritte
To a solution of fuming nitric acid (8 mL) and conc. H2SO4 (16 mL), was added 4-fluorobenzenesulfonyl chloride (1.3 g, 6.7 mmol) in small portions. The mixture was stirred at RT for 2 h. and then poured onto crushed ice (60 g) and extracted with dichloromethane (2×). The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated. The residue was dissolved in CH2Cl2 (30 mL) cooled to −40° C. and cyclopropylamine (388 mg, 6.8 mmol), followed by DIPEA (8 mmol) were added. After stirring at −40° C. for 2 h, the mixture was poured on 5% citric acid solution and extracted with dichloromethane. The organic layer was separated, and passed through a short pad of silica gel and concentrated in vacuo to afford N-cyclopropyl-4-fluoro-3-nitrobenzenesulfonamide (1.6 g, 92%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07547711B2 |
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| Quelldatensatz | uspto-grants-2009_06 |
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| ORD ID | ord-bd131697a92e497f93db29c2f1548092 |
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| Quellennotiz | uspto-grants-2009_06 |
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