HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277025Generated: October 25, 2026
Sodium Hydroxide → 5-Methyl-furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide
https://huagongshe.com/reaction/277025
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Methyl-2-furohydrazide | HCID 4159250 | — |
| Reactant | 2-(Phenylsulfonyl)-ethanimidic acid ethyl ester hydrochloride | HCID 70089441 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Methyl-furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide | HCID 86757844 | 82.8% |
Reaction Steps
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 hydroxide. 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. 17.8 g (0.078 Mol) of the resulting colorless oil was stirred together with 9.15 g (0.065 mol) 5-methyl-furan-2-carboxylic acid hydrazide in 115 ml chloroform for 24 hours at 50° C. The resulting precipitate was filtered off and dried. 17.3 g of 5-methyl-furan-2-carboxylic acid (1-amino-2-benzenesulfonyl-ethylidene)-hydrazide was obtained as white crystals. Mp.: 219-220° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06355653B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-7ecc062fc0854a2c86eb72796e15cb16 |
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| Source note | uspto-grants-2002_03 |
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