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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 432808Erstellt: 27. Oktober 2026

Sodium Thiosulfate → Ethyl 1-(3-(2-thienyl)propionyl)-3-piperidinecarboxylate

https://huagongshe.com/reaction/432808

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ThiosulfateHCID 24477—
EduktHydrazine hydrate (1:1)HCID 24654—
EduktSodium periodateHCID 23667635—
EduktEthyl 1-(3-(2-thienyl)acrylyl)-3-piperidinecarboxylateHCID 54520739—
KatalysatorAcetic AcidHCID 176—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 1-(3-(2-thienyl)propionyl)-3-piperidinecarboxylateHCID 1876028133,9%

Reaktionsschritte

Ethyl 1-(3-(2-thienyl)acrylyl)-3-piperidinecarboxylate (404.1 mg; 1.38 mmol) was suspended in dimethyl sulfoxide (8 ml). The suspension was treated with hydrazine hydrate (1.7 ml; 54.7 mmol), saturated aqueous copper sulfate solution (6 drops), and glacial acetic acid (6 drops). This mixture was then stirred at ambient temperature and sodium periodate (1.47 g; 6.87 mmol) in water (20 ml) was added dropwise. After stirring an additional 1 hour, the mixture was taken up between aqueous 5% sodium thiosulfate and dichloromethane. The dichloromethane was separated, dried with anhydrous potassium carbonate, and evaporated at ambient temperature under reduced pressure. The crude product was purified by reverse phase chromatography on a C18 column, eluting with 30:70 to 40:60 acetonitrile:water as a step gradient, giving ethyl 1-(3-(2-thienyl)propionyl)-3-piperidinecarboxylate (138 mg) as a colorless oil. MS m/z (positive ion) 296 (MH+; 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06664271B1
Quelldatensatzuspto-grants-2003_12
ORD IDord-c9ef6bf1c6b34bffa857fab1fd4863ec
Quellennotizuspto-grants-2003_12