HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277009Erstellt: 25. Oktober 2026
Sodium Hydroxide → Furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide
https://huagongshe.com/reaction/277009
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 2-Furancarboxylic acid, hydrazide | HCID 18731 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 2-(Phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride | HCID 70089441 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide | HCID 86757843 | — |
Reaktionsschritte
A suspension of 85.0 g (0.32 mol) 2-(phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride in 700 ml chloroform was treated with 320 ml 1N aqueous sodium hydoxide. 100 ml of a saturated aqueous sodiumbicarbonate solution was added and the mixture was extracted with chloroform. The extracts were combined and dried with sodium sulfate and the solvents were distilled off under reduced pressure. The resulting colorless oil was stirred together with 42.6 g (0.34 mol) 2-furancarboxylic acid hydrazide in 600 ml chloroform for 24 hours at 50° C. The resulting precipitate was filtered off and dried. A quantitative yield of furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide was obtained as pale crystals, mp. 195° C. (decomposition), MS m/e (%): 308 (M+H+, 100).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06355653B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-851ab4618392489f911aff3525372778 |
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| Quellennotiz | uspto-grants-2002_03 |
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