HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699239Generated: October 29, 2026
Water → 4-(Ethoxycarbonylamino)-thiophene-3-carboxaldehyde
https://huagongshe.com/reaction/1699239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 4-(ethoxycarbonylamino)-thiophene-3-carboxylate | HCID 14328004 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 4-(Ethoxycarbonylamino)-thiophene-3-carboxaldehyde | HCID 14672163 | — |
Reaction Steps
Into an ice-cold suspension of 12.9 g (0.34 mol) of lithium aluminium hydride in 800 ml of tert. butyl-methylether was added dropwise, at a reaction temperature of about 0° C., a solution of 59.1 g (0.258 mol) of methyl 4-(ethoxycarbonylamino)-thiophene-3-carboxylate in 200 ml of tert. butyl-methyl-ether, and the mixture was then stirred for a further 2 hours at 10° C. Then 13 ml of water, 13 ml of 2N aqueous sodium hydroxide solution and 39 ml of water were added dropwise one after another and the mixture was stirred for 1 hour at room temperature. It was filtered, and 500 g of activated manganese (IV) oxide were added in batches to the filtrate with stirring. After the completion of the reaction, which could be monitored by thin layer chromatography, the mixture was filtered again and the filtrate was then evaporated down in vacuo. The crystalline residue which solidified was further processed without any more purification. yield: 28.2 g (54.9% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06344449B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-ba804e8bf3dd4bf2a6d44c35fe092fa3 |
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| Source note | uspto-grants-2002_02 |
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