HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1457520Erstellt: 25. Oktober 2026
Sodium Hydroxide → methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate
https://huagongshe.com/reaction/1457520
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Stannous chloride dihydrate | HCID 61436 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate | HCID 10946074 | — |
| Edukt | Sodium Nitrite | HCID 23668193 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate | HCID 21716182 | 70% |
Reaktionsschritte
25.0 g (0.087 mol) of methyl 4-amino-2-(N-tert-butylsulfamoyl)benzoate are suspended in a mixture of 150 ml of concentrated HCl and 130 ml of water. A solution of 7.8 g (0.114 mol) of sodium nitrite is added dropwise at 0°-5° C. A small amount of undissolved constituents are filtered off cold and the still cold diazonium salt solution is allowed to run slowly at 0° C. into a suspension of 55.0 g (0.244 mol) of SnCl2.2H2O in 55 ml of concentrated HCl. The mixture is subsequently stirred for 30 minutes and is then left to stand for 15 hours, while cooling with ice. Most of the HCl is first neutralized by addition of 6N NaOH and the pH is then brought to about 6 with solid NaHCO3. The mixture is extracted several times with ethyl acetate, the extracts are dried and the solvent is removed in vacuo. After trituration of the residue with diisopropyl ether and drying, 18.3 g (70% of theory) of methyl 2-(N-tert-butylsulfamoyl)-4-hydrazinobenzoate of melting point 133°-136° C. are obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05849666 |
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| Quelldatensatz | uspto-grants-1998_12 |
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| ORD ID | ord-ca2a9994b9924578b1a6416fccba6964 |
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| Quellennotiz | uspto-grants-1998_12 |
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