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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 364495Erstellt: 25. Oktober 2026

Propargyl bromide → Ethyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetate

https://huagongshe.com/reaction/364495

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPropargyl bromideHCID 7842—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 2-(2-tritylamino-4-thiazolyl)-2-hydroxyiminoacetateHCID 6802348—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetateHCID 5412433577%

Reaktionsschritte

Propargyl bromide (4.16 g.) was added to a suspension of ethyl 2-(2-tritylaminothiazol-4-yl)-2-hydroxyiminoacetate (syn isomer, 10 g.), potassium carbonate (4.84 g.) and N,N-dimethylformamide (22 ml.) under atmosphere of nitrogen gas and stirred at room temperature for 100 minutes. The insoluble substance was filtered off and washed with a little of N,N-dimethylformamide. The filtrate and washing solution were combined together, and water (400 ml.) was added to the solution. After the suspension was extracted with ethyl acetate (400 ml.), the extract was washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. After treating the solution with activated charcoal, the solution was concentrated in vacuo. The residue was triturated with diisopropyl ether. The precipitates were collected by filtration, and washed with diisopropyl ether to give ethyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetate (syn isomer, 8.34 g.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04604456
Quelldatensatzuspto-grants-1986_08
ORD IDord-090bfe868c564c2fa315d6288ef2a960
Quellennotizuspto-grants-1986_08