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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant4-chlorothiophene-2-carbaldehydeHCID 10997182—
SolventEthanolHCID 702—
ProductEthyl 3-chloro-4H-thieno[3,2-b]pyrrole-5-carboxylateHCID 57348924—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06576653B2
Source datasetuspto-grants-2003_06
ORD IDord-21601d6471cf4d84ae9396fbf637e448
Source noteuspto-grants-2003_06