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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453584Generated: October 30, 2026

Ammonium Chloride → HCID 59411378, compound

https://huagongshe.com/reaction/453584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantAcetic acid, azido-, ethyl esterHCID 69480—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 86643546HCID 86643546—
SolventEthanolHCID 702—
ProductHCID 59411378HCID 5941137810%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492405B2
Source datasetuspto-grants-2013_07
ORD IDord-a1f0306e8cf64fd68d4bb6bab94f6f6f
Source noteuspto-grants-2013_07