HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453584Generated: October 30, 2026
Ammonium Chloride → HCID 59411378, compound
https://huagongshe.com/reaction/453584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 86643546 | HCID 86643546 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59411378 | HCID 59411378 | 10% |
Reaction Steps
To a solution (20 mL) of sodium ethoxide (0.68 g) in ethanol was added dropwise a mixture of benzyl (5-formyl-2-methyl-3-thienyl)methylcarbamate (0.72 g) and ethyl azidoacetate (1.3 g) under ice-cooling. After the completion of the dropwise addition, the mixture was stirred for 1 hr. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was concentrated. The obtained residue was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The obtained residue was dissolved in toluene (20 mL), and the mixture was stirred at 110° C. for 2 hr. The reaction mixture was concentrated, and the residue was subjected to silica gel column chromatography to give ethyl 3-{[(benzyloxy)carbonyl](methyl)amino}-2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate (91 mg, yield 10%) as colorless crystals from a fraction eluted with ethyl acetate-hexane (1:3, volume ratio). melting point 122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492405B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-a1f0306e8cf64fd68d4bb6bab94f6f6f |
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| Source note | uspto-grants-2013_07 |
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