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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1709125Erstellt: 27. Oktober 2026

Triethylamine → 3-(7-Chloro-2,3-dihydro-2-methyl-4-benzofuranyl)-1-methylimidazolidine-2,4-dione

https://huagongshe.com/reaction/1709125

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl N-methylaminoacetate hydrochlorideHCID 171173—
Edukt7-Chloro-2,3-dihydro-4-isocyanato-2-methylbenzofuranHCID 53718402—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-(7-Chloro-2,3-dihydro-2-methyl-4-benzofuranyl)-1-methylimidazolidine-2,4-dioneHCID 67926701—

Reaktionsschritte

2.30 g of sarcosine ethyl ester hydrochloride was added over 5 minutes to a mixture of 2.10 g of 34A, 1.52 g of triethylamine and 60 mL of methylene chloride, under nitrogen at 25°-30° C. The mixture was stirred at room temperature for 24 hours, then diluted with 100 mL of methylene chloride, washed with water, then brine, dried (MgSO4) and stripped of solvent. The residue was dissolved in 70 mL of a 1:1 v:v mixture of ethanol and 2N hydrochloric acid. The solution was refluxed for 4 hours, the resulting mixture was stirred at room temperature overnight, stripped of volatiles, diluted with water and extracted with methylene chloride. The extract was dried (MgSO4) and stripped of solvent. The residue was purified by flash chromatography over silica gel with a 1:2 v:v mixture of hexane and ethyl acetate as eluent to give the title compound, as a glass/sticky solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04948418
Quelldatensatzuspto-grants-1990_08
ORD IDord-a39cad90a0c4422e9b4ca4fb11c6d085
Quellennotizuspto-grants-1990_08