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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494279Generated: November 3, 2026

Ammonia → 1-Carbamoyl-3-(trimethylstannyl)dibenzofuran

https://huagongshe.com/reaction/1494279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 19737925HCID 19737925—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product1-Carbamoyl-3-(trimethylstannyl)dibenzofuranHCID 1988783388.4%

Reaction Steps

To a stirred solution of the stannane 306 (1.1 g, 2.96 mmol) in anhydrous acetonitrile (5 mL) and THF (15 mL) under a nitrogen atmosphere was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.13 g, 5.9 mmol) and 1-hydroxybenzotriazole hydrate (1.2 g, 8.9 mmol). The solution was stirred 30 min., then 11 mL of a 2.6 M ethanolic ammonia solution was added. The resulting milky white solution was stirred an additional 30 min. before being quenched with saturated aqueous ammonium chloride. The solvents were removed under vacuum and the residue taken up in ether (75 mL) and EtOAc (75 mL). The solution was washed with water (3 times) and brine (2 times), then dried with magnesium sulfate and filtered. The solution was concentrated under vacuum and the residue was purified by flash chromatography (silica gel, 35% EtOAc in hexanes) to provide 979 mg (88% yield) of stannane 307 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025008
Source datasetuspto-grants-1991_06
ORD IDord-1544d2a324d44ec9a61177a7642b0e36
Source noteuspto-grants-1991_06