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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184697Generated: October 29, 2026

Ammonium Chloride → 3-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acid

https://huagongshe.com/reaction/2184697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
SolventEthanolHCID 702—
Product3-Bromo-4H-thieno[3,2-b]pyrrole-5-carboxylic acidHCID 22556498—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-Bromo-thiophene-2-carbaldehyde 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 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 numberUS06399601B1
Source datasetuspto-grants-2002_06
ORD IDord-1f73782a12fb400685757f9eafe392e8
Source noteuspto-grants-2002_06