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HRID 544441Erstellt: 24. Oktober 2026

Potassium Carbonate → [5-phenoxy-(1,2,4)-thiadiazol-3-yl]-methyl (1R,3R)2,2-dimethyl-3-(2-methyl-1-propenyl)-cyclopropane-1-carboxylate

https://huagongshe.com/de/reaction/544441

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Eduktchrysanthemic acid d-trans-formHCID 16747—
Edukt18-Crown-6HCID 28557—
Edukt3-Chloromethyl-5-phenoxy-(1,2,4)-thiadiazoleHCID 13106144—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt[5-phenoxy-(1,2,4)-thiadiazol-3-yl]-methyl (1R,3R)2,2-dimethyl-3-(2-methyl-1-propenyl)-cyclopropane-1-carboxylateHCID 5729377830,9%

Reaktionsschritte

A mixture of 4.5 g of 3-chloromethyl-5-phenoxy-(1,2,4)-thiadiazole, 3.7 g of (1R,3R) 2,2-dimethyl-3-(2-methyl-1-propenyl)-cyclopropane-1-carboxylic acid, 50 ml of methyl ethyl ketone, 3.2 g of potassium carbonate and 0.1 gof 1,4,7,10,13,16-hexaoxacyclooctadecane was refluxed for 18 hours and was cooled and filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution withbenzene yielded 2.2 g of [5-phenoxy-(1,2,4)-thiadiazol-3-yl]-methyl (1R,3R)2,2-dimethyl-3-(2-methyl-1-propenyl)-cyclopropane-1-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04450169
Quelldatensatzuspto-grants-1984_05
ORD IDord-ec9ce7cad0d84bfcb864028692f5b823
Quellennotizuspto-grants-1984_05