HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368980Generated: November 2, 2026
Ammonium Chloride → Ethyl 3-chloro-4H-thieno[3,2-b]pyrrole-5-carboxylate
https://huagongshe.com/reaction/1368980
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Acetic acid, azido-, ethyl ester | HCID 69480 | — |
| Reactant | 4-chlorothiophene-2-carbaldehyde | HCID 10997182 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 3-chloro-4H-thieno[3,2-b]pyrrole-5-carboxylate | HCID 57348924 | — |
Reaction Steps
4-Chloro-thiophene-2-carbaldehyde (Iriarte, J.; Martinez, E.; Muchowski, J. M., J. Heterocycl. Chem., 13: 393-4 (1976)) was annulated according to Procedure H (aldehyde and azido-acetic acid ethyl ester added as ethanol solution (1.2 M of ester) such that reaction temperature maintained at 0° C.; reaction mixture allowed to warm to 10° C., stirred for 1.5 h, poured into cold saturated aqueous NH4Cl; after ether extractions, combined acrylate organic phases washed with water until aqueous phase was neutral; acrylate not purified).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06576653B2 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-21601d6471cf4d84ae9396fbf637e448 |
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| Source note | uspto-grants-2003_06 |
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